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dbVar

Database of genomic structural variation

nsv5972904

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: 145 SVs from 34 studies. See in: genome view

Submitted genomic50,340,891-50,340,891

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972904	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	50,340,891	50,340,891
nsv5972904	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	50,633,088	50,633,088

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17370941	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17370941	Submitted genomic		NC_000015.10:g.503 40891_50340892ins2 43	GRCh38 (hg38)		NC_000015.10	Chr15	50,340,891	50,340,891
nssv17370941	Remapped	Perfect	NC_000015.9:g.5063 3088_50633089ins24 3	GRCh37.p13	First Pass	NC_000015.9	Chr15	50,633,088	50,633,088

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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