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dbVar

Database of genomic structural variation

nsv5965436

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 234 SVs from 24 studies. See in: genome view

Submitted genomic124,602,188-124,602,188

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965436	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	124,602,188	124,602,188
nsv5965436	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	125,614,429	125,614,429

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17447525	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17447525	Submitted genomic		NC_000008.11:g.124 602188_124602189in s56	GRCh38 (hg38)		NC_000008.11	Chr8	124,602,188	124,602,188
nssv17447525	Remapped	Perfect	NC_000008.10:g.125 614429_125614430in s56	GRCh37.p13	First Pass	NC_000008.10	Chr8	125,614,429	125,614,429

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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