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dbVar

Database of genomic structural variation

nsv6021596

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:328

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: 208 SVs from 26 studies. See in: genome view

Submitted genomic124,929,697-124,930,024

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6021596	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	124,929,697	124,930,024
nsv6021596	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	124,799,593	124,799,920

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17605408	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17605408	Submitted genomic		NC_000011.10:g.124 929697_124930024de l	GRCh38 (hg38)		NC_000011.10	Chr11	124,929,697	124,930,024
nssv17605408	Remapped	Perfect	NC_000011.9:g.1247 99593_124799920del	GRCh37.p13	First Pass	NC_000011.9	Chr11	124,799,593	124,799,920

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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