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dbVar

Database of genomic structural variation

nsv5576866

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:177

Publication(s):Ebert et al. 2021

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: 262 SVs from 42 studies. See in: genome view

Submitted genomic37,295,928-37,296,104

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5576866	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	37,295,928	37,296,104
nsv5576866	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	37,296,030	37,296,206

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17128603	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17128603	Submitted genomic		NC_000005.10:g.372 95928_37296104delG	GRCh38 (hg38)		NC_000005.10	Chr5	37,295,928	37,296,104
nssv17128603	Remapped	Perfect	NC_000005.9:g.3729 6030_37296206delG	GRCh37.p13	First Pass	NC_000005.9	Chr5	37,296,030	37,296,206

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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