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dbVar

Database of genomic structural variation

nsv5657881

Organism: Homo sapiens

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

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

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: 106 SVs from 17 studies. See in: genome view

Submitted genomic68,496,010-68,496,010

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657881	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	68,496,010	68,496,010
nsv5657881	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	66,492,151	66,492,151

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17094590	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17094590	Submitted genomic		NC_000017.11:g.684 96010_68496011ins6 64	GRCh38 (hg38)		NC_000017.11	Chr17	68,496,010	68,496,010
nssv17094590	Remapped	Perfect	NC_000017.10:g.664 92151_66492152ins6 64	GRCh37.p13	First Pass	NC_000017.10	Chr17	66,492,151	66,492,151

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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