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dbVar

Database of genomic structural variation

nsv5922144

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,153

Publication(s):Almarri et al. 2020

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: 471 SVs from 44 studies. See in: genome view

Submitted genomic166,748,590-166,749,742

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922144	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	166,748,590	166,749,742
nsv5922144	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	167,162,078	167,163,230

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17427081	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17427081	Submitted genomic		NC_000006.12:g.166 748590_166749742de l	GRCh38 (hg38)		NC_000006.12	Chr6	166,748,590	166,749,742
nssv17427081	Remapped	Perfect	NC_000006.11:g.167 162078_167163230de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	167,162,078	167,163,230

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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