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dbVar

Database of genomic structural variation

nsv5937483

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:144

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: 113 SVs from 27 studies. See in: genome view

Submitted genomic57,628,892-57,629,035

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5937483	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	57,628,892	57,629,035
nsv5937483	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	57,662,804	57,662,947

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17386097	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17386097	Submitted genomic		NC_000016.10:g.576 28892_57629035del	GRCh38 (hg38)		NC_000016.10	Chr16	57,628,892	57,629,035
nssv17386097	Remapped	Perfect	NC_000016.9:g.5766 2804_57662947del	GRCh37.p13	First Pass	NC_000016.9	Chr16	57,662,804	57,662,947

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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