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dbVar

Database of genomic structural variation

nsv5642172

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: 225 SVs from 38 studies. See in: genome view

Submitted genomic167,130,970-167,130,970

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642172	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	167,130,970	167,130,970
nsv5642172	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	167,544,458	167,544,458

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17156537	insertion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17156537	Submitted genomic		NC_000006.12:g.167 130970_167130971in s62	GRCh38 (hg38)		NC_000006.12	Chr6	167,130,970	167,130,970
nssv17156537	Remapped	Perfect	NC_000006.11:g.167 544458_167544459in s62	GRCh37.p13	First Pass	NC_000006.11	Chr6	167,544,458	167,544,458

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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