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dbVar

Database of genomic structural variation

nsv5950390

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

Submitted genomic98,119,801-98,119,801

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5950390	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	98,119,801	98,119,801
nsv5950390	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	100,882,083	100,882,083

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17447647	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17447647	Submitted genomic		NC_000009.12:g.981 19801_98119802ins1 13	GRCh38 (hg38)		NC_000009.12	Chr9	98,119,801	98,119,801
nssv17447647	Remapped	Perfect	NC_000009.11:g.100 882083_100882084in s113	GRCh37.p13	First Pass	NC_000009.11	Chr9	100,882,083	100,882,083

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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