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dbVar

Database of genomic structural variation

nsv5944786

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:106

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: 122 SVs from 37 studies. See in: genome view

Submitted genomic65,060,406-65,060,511

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944786	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	65,060,406	65,060,511
nsv5944786	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	65,527,124	65,527,229

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17377645	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17377645	Submitted genomic		NC_000014.9:g.6506 0406_65060511del	GRCh38 (hg38)		NC_000014.9	Chr14	65,060,406	65,060,511
nssv17377645	Remapped	Perfect	NC_000014.8:g.6552 7124_65527229del	GRCh37.p13	First Pass	NC_000014.8	Chr14	65,527,124	65,527,229

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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