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dbVar

Database of genomic structural variation

nsv5958345

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

Submitted genomic51,015,837-51,015,837

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958345	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	51,015,837	51,015,837
nsv5958345	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	51,053,268	51,053,268

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418373	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418373	Submitted genomic		NC_000003.12:g.510 15837_51015838ins2 40	GRCh38 (hg38)		NC_000003.12	Chr3	51,015,837	51,015,837
nssv17418373	Remapped	Perfect	NC_000003.11:g.510 53268_51053269ins2 40	GRCh37.p13	First Pass	NC_000003.11	Chr3	51,053,268	51,053,268

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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