nsv6622955

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:54
Validation:Not tested
Clinical Assertions: No
Region Size:99,916

Publication(s):Zarrei et al. 2023

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 4037 SVs from 94 studies. See in: genome view

Remapped(Score: Perfect):22,080,637-22,180,552

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6622955	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nsv6622955	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	22,368,588	22,468,503

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18282428	duplication	OSC2163	SNP array	Probe signal intensity	12
nssv18282607	duplication	OSC2070	SNP array	Probe signal intensity	9
nssv18283025	duplication	OSC2381	SNP array	Probe signal intensity	nssv18283656, nssv18283026
nssv18283211	duplication	OSC2306	SNP array	Probe signal intensity	6
nssv18283920	duplication	OSC2363	SNP array	Probe signal intensity	10
nssv18284403	duplication	OSC2528	SNP array	Probe signal intensity	7
nssv18284842	duplication	OSC2578	SNP array	Probe signal intensity	10
nssv18285111	duplication	OSC2529	SNP array	Probe signal intensity	5
nssv18285380	duplication	OSC2719	SNP array	Probe signal intensity	8
nssv18285410	duplication	OSC2742	SNP array	Probe signal intensity	5
nssv18286760	duplication	OSC3048	SNP array	Probe signal intensity	11
nssv18287074	duplication	OSC3108	SNP array	Probe signal intensity	7
nssv18287131	duplication	OSC3143	SNP array	Probe signal intensity	6
nssv18287875	duplication	OSC3173	SNP array	Probe signal intensity	6
nssv18287905	duplication	OSC3190	SNP array	Probe signal intensity	6
nssv18287943	duplication	OSC3211	SNP array	Probe signal intensity	nssv18288501, nssv18287942, nssv18288172
nssv18289313	duplication	OSC3543	SNP array	Probe signal intensity	5
nssv18289621	duplication	OSC3590	SNP array	Probe signal intensity	7
nssv18291306	duplication	OSC3671	SNP array	Probe signal intensity	7
nssv18291551	duplication	OSC3822	SNP array	Probe signal intensity	7
nssv18291639	duplication	OSC3886	SNP array	Probe signal intensity	7
nssv18291933	duplication	OSC3931	SNP array	Probe signal intensity	10
nssv18294254	duplication	OSC4257	SNP array	Probe signal intensity	12
nssv18295602	duplication	OSC4569	SNP array	Probe signal intensity	9
nssv18296276	duplication	OSC4578	SNP array	Probe signal intensity	5
nssv18296908	duplication	OSC4845	SNP array	Probe signal intensity	10
nssv18297677	duplication	OSC4909	SNP array	Probe signal intensity	10
nssv18297699	duplication	OSC4929	SNP array	Probe signal intensity	7
nssv18298043	duplication	OSC5014	SNP array	Probe signal intensity	5
nssv18298410	duplication	OSC5036	SNP array	Probe signal intensity	8
nssv18298575	duplication	OSC4918	SNP array	Probe signal intensity	nssv18298574, nssv18297683
nssv18299328	duplication	OSC5272	SNP array	Probe signal intensity	14
nssv18300196	duplication	OSC5422	SNP array	Probe signal intensity	5
nssv18300915	duplication	OSC0567	SNP array	Probe signal intensity	nssv18300314
nssv18302113	duplication	OSC5717	SNP array	Probe signal intensity	6
nssv18310873	duplication	OSC0077	SNP array	Probe signal intensity	7
nssv18312188	duplication	OSC0779	SNP array	Probe signal intensity	6
nssv18320087	duplication	OSC1086	SNP array	Probe signal intensity	11
nssv18320425	duplication	OSC1060	SNP array	Probe signal intensity	7
nssv18320939	duplication	OSC1039	SNP array	Probe signal intensity	8
nssv18321319	duplication	OSC1302	SNP array	Probe signal intensity	9
nssv18322503	duplication	OSC1493	SNP array	Probe signal intensity	10
nssv18322890	duplication	OSC1502	SNP array	Probe signal intensity	7
nssv18322925	duplication	OSC1340	SNP array	Probe signal intensity	8
nssv18323634	duplication	OSC1652	SNP array	Probe signal intensity	7
nssv18324959	duplication	OSC1917	SNP array	Probe signal intensity	5
nssv18325311	duplication	OSC1913	SNP array	Probe signal intensity	nssv18325859, nssv18325858, nssv18325312
nssv18325521	duplication	OSC1855	SNP array	Probe signal intensity	7
nssv18325535	duplication	OSC1865	SNP array	Probe signal intensity	5
nssv18325715	duplication	OSC1812	SNP array	Probe signal intensity	13
nssv18325865	duplication	OSC1921	SNP array	Probe signal intensity	5
nssv18326182	duplication	OSC1976	SNP array	Probe signal intensity	nssv18326084, nssv18325972
nssv18326188	duplication	OSC1982	SNP array	Probe signal intensity	7
nssv18326202	duplication	OSC1991	SNP array	Probe signal intensity	5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18282428	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18282607	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18283025	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18283211	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18283920	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18284403	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18284842	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18285111	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18285380	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18285410	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18286760	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18287074	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18287131	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18287875	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18287905	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18287943	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18289313	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18289621	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18291306	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18291551	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18291639	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18291933	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18294254	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18295602	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18296276	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18296908	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18297677	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18297699	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18298043	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18298410	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18298575	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18299328	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18300196	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18300915	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18302113	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18310873	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18312188	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18320087	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18320425	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18320939	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18321319	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18322503	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18322890	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18322925	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18323634	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18324959	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18325311	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18325521	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18325535	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18325715	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18325865	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18326182	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18326188	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18326202	Remapped	Perfect	NC_000015.10:g.(?_ 22080637)_(2218055 2_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	22,080,637	22,180,552
nssv18282428	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18282607	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18283025	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18283211	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18283920	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18284403	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18284842	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18285111	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18285380	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18285410	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18286760	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18287074	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18287131	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18287875	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18287905	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18287943	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18289313	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18289621	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18291306	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18291551	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18291639	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18291933	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18294254	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18295602	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18296276	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18296908	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18297677	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18297699	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18298043	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18298410	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18298575	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18299328	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18300196	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18300915	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18302113	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18310873	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18312188	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18320087	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18320425	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18320939	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18321319	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18322503	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18322890	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18322925	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18323634	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503
nssv18324959	Submitted genomic		NC_000015.9:g.(?_2 2368588)_(22468503 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	22,368,588	22,468,503

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dbVar

Database of genomic structural variation

nsv6622955

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant