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dbVar

Database of genomic structural variation

nsv5969247

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: 208 SVs from 25 studies. See in: genome view

Submitted genomic97,291,900-97,291,900

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5969247	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	97,291,900	97,291,900
nsv5969247	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	97,944,154	97,944,154

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17376917	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17376917	Submitted genomic		NC_000013.11:g.972 91900_97291901ins2 57	GRCh38 (hg38)		NC_000013.11	Chr13	97,291,900	97,291,900
nssv17376917	Remapped	Perfect	NC_000013.10:g.979 44154_97944155ins2 57	GRCh37.p13	First Pass	NC_000013.10	Chr13	97,944,154	97,944,154

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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