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dbVar

Database of genomic structural variation

nsv5960881

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 31 studies. See in: genome view

Submitted genomic10,070,476-10,070,476

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960881	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	10,070,476	10,070,476
nsv5960881	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	10,112,160	10,112,160

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17390873	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17390873	Submitted genomic		NC_000003.12:g.100 70476_10070477ins1 64	GRCh38 (hg38)		NC_000003.12	Chr3	10,070,476	10,070,476
nssv17390873	Remapped	Perfect	NC_000003.11:g.101 12160_10112161ins1 64	GRCh37.p13	First Pass	NC_000003.11	Chr3	10,112,160	10,112,160

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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