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dbVar

Database of genomic structural variation

nsv5867713

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:14,101

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: 616 SVs from 75 studies. See in: genome view

Submitted genomic16,032,248-16,046,348

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5867713	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	16,032,248	16,046,348
nsv5867713	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	16,358,743	16,372,843

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17366781	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17366781	Submitted genomic		NC_000001.11:g.160 32248_16046348del	GRCh38 (hg38)		NC_000001.11	Chr1	16,032,248	16,046,348
nssv17366781	Remapped	Perfect	NC_000001.10:g.163 58743_16372843del	GRCh37.p13	First Pass	NC_000001.10	Chr1	16,358,743	16,372,843

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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