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dbVar

Database of genomic structural variation

nsv5975622

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: 187 SVs from 43 studies. See in: genome view

Submitted genomic33,820,898-33,820,898

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5975622	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	33,820,898	33,820,898
nsv5975622	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	34,113,099	34,113,099

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17377949	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17377949	Submitted genomic		NC_000015.10:g.338 20898_33820899ins5 56	GRCh38 (hg38)		NC_000015.10	Chr15	33,820,898	33,820,898
nssv17377949	Remapped	Perfect	NC_000015.9:g.3411 3099_34113100ins55 6	GRCh37.p13	First Pass	NC_000015.9	Chr15	34,113,099	34,113,099

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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