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dbVar

Database of genomic structural variation

nsv6006213

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:3,252

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: 151 SVs from 25 studies. See in: genome view

Submitted genomic123,012,401-123,015,652

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6006213	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	123,012,401	123,015,652
nsv6006213	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	124,771,917	124,775,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17587844	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17587844	Submitted genomic		NC_000010.11:g.123 012401_123015652de l	GRCh38 (hg38)		NC_000010.11	Chr10	123,012,401	123,015,652
nssv17587844	Remapped	Perfect	NC_000010.10:g.124 771917_124775168de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,771,917	124,775,168

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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