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dbVar

Database of genomic structural variation

nsv5962493

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: 91 SVs from 19 studies. See in: genome view

Submitted genomic14,184,298-14,184,298

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5962493	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	14,184,298	14,184,298
nsv5962493	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	14,226,297	14,226,297

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17363127	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17363127	Submitted genomic		NC_000010.11:g.141 84298_14184299ins2 62	GRCh38 (hg38)		NC_000010.11	Chr10	14,184,298	14,184,298
nssv17363127	Remapped	Perfect	NC_000010.10:g.142 26297_14226298ins2 62	GRCh37.p13	First Pass	NC_000010.10	Chr10	14,226,297	14,226,297

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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