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dbVar

Database of genomic structural variation

nsv5902376

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:133

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: 151 SVs from 43 studies. See in: genome view

Submitted genomic87,408,455-87,408,587

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5902376	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	87,408,455	87,408,587
nsv5902376	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	88,118,173	88,118,305

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448730	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448730	Submitted genomic		NC_000006.12:g.874 08455_87408587del	GRCh38 (hg38)		NC_000006.12	Chr6	87,408,455	87,408,587
nssv17448730	Remapped	Perfect	NC_000006.11:g.881 18173_88118305del	GRCh37.p13	First Pass	NC_000006.11	Chr6	88,118,173	88,118,305

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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