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dbVar

Database of genomic structural variation

nsv5960985

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

Submitted genomic152,720,034-152,720,034

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960985	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	152,720,034	152,720,034
nsv5960985	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	153,576,548	153,576,548

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17398721	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17398721	Submitted genomic		NC_000002.12:g.152 720034_152720035in s95	GRCh38 (hg38)		NC_000002.12	Chr2	152,720,034	152,720,034
nssv17398721	Remapped	Perfect	NC_000002.11:g.153 576548_153576549in s95	GRCh37.p13	First Pass	NC_000002.11	Chr2	153,576,548	153,576,548

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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