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dbVar

Database of genomic structural variation

nsv5642390

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: 240 SVs from 40 studies. See in: genome view

Submitted genomic167,130,932-167,130,932

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642390	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	167,130,932	167,130,932
nsv5642390	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	167,544,420	167,544,420

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149638	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17149638	Submitted genomic		NC_000006.12:g.167 130932_167130933in s124	GRCh38 (hg38)		NC_000006.12	Chr6	167,130,932	167,130,932
nssv17149638	Remapped	Perfect	NC_000006.11:g.167 544420_167544421in s124	GRCh37.p13	First Pass	NC_000006.11	Chr6	167,544,420	167,544,420

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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