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dbVar

Database of genomic structural variation

nsv5960688

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: 127 SVs from 26 studies. See in: genome view

Submitted genomic109,187,443-109,187,443

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960688	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	109,187,443	109,187,443
nsv5960688	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	111,949,723	111,949,723

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17432063	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17432063	Submitted genomic		NC_000009.12:g.109 187443_109187444in s318	GRCh38 (hg38)		NC_000009.12	Chr9	109,187,443	109,187,443
nssv17432063	Remapped	Perfect	NC_000009.11:g.111 949723_111949724in s318	GRCh37.p13	First Pass	NC_000009.11	Chr9	111,949,723	111,949,723

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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