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dbVar

Database of genomic structural variation

nsv6008554

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:54

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: 143 SVs from 41 studies. See in: genome view

Submitted genomic31,132,407-31,132,460

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6008554	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	31,132,407	31,132,460
nsv6008554	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	31,100,184	31,100,237

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17565980	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17565980	Submitted genomic		NC_000006.12:g.311 32407_31132460del	GRCh38 (hg38)		NC_000006.12	Chr6	31,132,407	31,132,460
nssv17565980	Remapped	Perfect	NC_000006.11:g.311 00184_31100237del	GRCh37.p13	First Pass	NC_000006.11	Chr6	31,100,184	31,100,237

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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