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dbVar

Database of genomic structural variation

nsv6002937

Organism: Homo sapiens

Study:nstd212 (Wu 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:78

Publication(s):Wu 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: 182 SVs from 17 studies. See in: genome view

Submitted genomic38,038,372-38,038,449

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6002937	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	38,038,372	38,038,449
nsv6002937	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	37,895,890	37,895,967

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17568336	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17568336	Submitted genomic		NC_000008.11:g.380 38372_38038449del	GRCh38 (hg38)		NC_000008.11	Chr8	38,038,372	38,038,449
nssv17568336	Remapped	Perfect	NC_000008.10:g.378 95890_37895967del	GRCh37.p13	First Pass	NC_000008.10	Chr8	37,895,890	37,895,967

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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