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dbVar

Database of genomic structural variation

nsv5966013

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: 153 SVs from 33 studies. See in: genome view

Submitted genomic131,130,150-131,130,150

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966013	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	131,130,150	131,130,150
nsv5966013	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	134,005,537	134,005,537

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437501	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437501	Submitted genomic		NC_000009.12:g.131 130150_131130151in s142	GRCh38 (hg38)		NC_000009.12	Chr9	131,130,150	131,130,150
nssv17437501	Remapped	Perfect	NC_000009.11:g.134 005537_134005538in s142	GRCh37.p13	First Pass	NC_000009.11	Chr9	134,005,537	134,005,537

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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