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dbVar

Database of genomic structural variation

nsv5639010

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: 182 SVs from 31 studies. See in: genome view

Submitted genomic181,215,302-181,215,302

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5639010	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	181,215,302	181,215,302
nsv5639010	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	180,642,302	180,642,302

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17138025	insertion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17138025	Submitted genomic		NC_000005.10:g.181 215302_181215303in s80	GRCh38 (hg38)		NC_000005.10	Chr5	181,215,302	181,215,302
nssv17138025	Remapped	Perfect	NC_000005.9:g.1806 42302_180642303ins 80	GRCh37.p13	First Pass	NC_000005.9	Chr5	180,642,302	180,642,302

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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