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dbVar

Database of genomic structural variation

nsv5606442

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

Submitted genomic156,895,955-156,895,955

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5606442	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	156,895,955	156,895,955
nsv5606442	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	156,865,747	156,865,747

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17061193	insertion	SAMN00001229	Sequencing	Sequence alignment	1,149

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17061193	Submitted genomic		NC_000001.11:g.156 895955_156895956in s1917	GRCh38 (hg38)		NC_000001.11	Chr1	156,895,955	156,895,955
nssv17061193	Remapped	Perfect	NC_000001.10:g.156 865747_156865748in s1917	GRCh37.p13	First Pass	NC_000001.10	Chr1	156,865,747	156,865,747

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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