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dbVar

Database of genomic structural variation

nsv5963619

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: 213 SVs from 39 studies. See in: genome view

Submitted genomic55,911,192-55,911,192

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5963619	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	55,911,192	55,911,192
nsv5963619	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	56,823,751	56,823,751

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17435431	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17435431	Submitted genomic		NC_000008.11:g.559 11192_55911193ins5 0	GRCh38 (hg38)		NC_000008.11	Chr8	55,911,192	55,911,192
nssv17435431	Remapped	Perfect	NC_000008.10:g.568 23751_56823752ins5 0	GRCh37.p13	First Pass	NC_000008.10	Chr8	56,823,751	56,823,751

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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