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dbVar

Database of genomic structural variation

nsv5959591

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: 94 SVs from 20 studies. See in: genome view

Submitted genomic69,761,004-69,761,004

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5959591	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	69,761,004	69,761,004
nsv5959591	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	69,988,136	69,988,136

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17408528	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17408528	Submitted genomic		NC_000002.12:g.697 61004_69761005ins6 9	GRCh38 (hg38)		NC_000002.12	Chr2	69,761,004	69,761,004
nssv17408528	Remapped	Perfect	NC_000002.11:g.699 88136_69988137ins6 9	GRCh37.p13	First Pass	NC_000002.11	Chr2	69,988,136	69,988,136

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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