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dbVar

Database of genomic structural variation

nsv5642742

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert 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 34 studies. See in: genome view

Submitted genomic160,219,096-160,219,096

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642742	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	160,219,096	160,219,096
nsv5642742	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	160,640,128	160,640,128

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149598	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17149598	Submitted genomic		NC_000006.12:g.160 219096_160219097in s3403	GRCh38 (hg38)		NC_000006.12	Chr6	160,219,096	160,219,096
nssv17149598	Remapped	Perfect	NC_000006.11:g.160 640128_160640129in s3403	GRCh37.p13	First Pass	NC_000006.11	Chr6	160,640,128	160,640,128

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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