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dbVar

Database of genomic structural variation

nsv5958004

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: 117 SVs from 22 studies. See in: genome view

Submitted genomic92,955,204-92,955,204

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958004	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	92,955,204	92,955,204
nsv5958004	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	93,420,761	93,420,761

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17398148	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17398148	Submitted genomic		NC_000001.11:g.929 55204_92955205ins1 92	GRCh38 (hg38)		NC_000001.11	Chr1	92,955,204	92,955,204
nssv17398148	Remapped	Perfect	NC_000001.10:g.934 20761_93420762ins1 92	GRCh37.p13	First Pass	NC_000001.10	Chr1	93,420,761	93,420,761

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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