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dbVar

Database of genomic structural variation

nsv5640114

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: 117 SVs from 22 studies. See in: genome view

Submitted genomic158,693,698-158,693,698

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5640114	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	158,693,698	158,693,698
nsv5640114	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	159,114,730	159,114,730

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17153354	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17153354	Submitted genomic		NC_000006.12:g.158 693698_158693699in s125	GRCh38 (hg38)		NC_000006.12	Chr6	158,693,698	158,693,698
nssv17153354	Remapped	Perfect	NC_000006.11:g.159 114730_159114731in s125	GRCh37.p13	First Pass	NC_000006.11	Chr6	159,114,730	159,114,730

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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