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dbVar

Database of genomic structural variation

nsv5960529

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: 243 SVs from 33 studies. See in: genome view

Submitted genomic174,497,568-174,497,568

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960529	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	174,497,568	174,497,568
nsv5960529	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	175,418,719	175,418,719

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17416057	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17416057	Submitted genomic		NC_000004.12:g.174 497568_174497569in s189	GRCh38 (hg38)		NC_000004.12	Chr4	174,497,568	174,497,568
nssv17416057	Remapped	Perfect	NC_000004.11:g.175 418719_175418720in s189	GRCh37.p13	First Pass	NC_000004.11	Chr4	175,418,719	175,418,719

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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