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dbVar

Database of genomic structural variation

nsv5891353

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:390

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: 193 SVs from 40 studies. See in: genome view

Submitted genomic89,096,880-89,097,269

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5891353	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	89,096,880	89,097,269
nsv5891353	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	90,018,031	90,018,420

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423510	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423510	Submitted genomic		NC_000004.12:g.890 96880_89097269del	GRCh38 (hg38)		NC_000004.12	Chr4	89,096,880	89,097,269
nssv17423510	Remapped	Perfect	NC_000004.11:g.900 18031_90018420del	GRCh37.p13	First Pass	NC_000004.11	Chr4	90,018,031	90,018,420

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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