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dbVar

Database of genomic structural variation

nsv5617342

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: 120 SVs from 21 studies. See in: genome view

Submitted genomic93,877,695-93,877,695

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5617342	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	93,877,695	93,877,695
nsv5617342	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	94,343,251	94,343,251

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17067150	insertion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17067150	Submitted genomic		NC_000001.11:g.938 77695_93877696ins4 98	GRCh38 (hg38)		NC_000001.11	Chr1	93,877,695	93,877,695
nssv17067150	Remapped	Perfect	NC_000001.10:g.943 43251_94343252ins4 98	GRCh37.p13	First Pass	NC_000001.10	Chr1	94,343,251	94,343,251

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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