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dbVar

Database of genomic structural variation

nsv5592627

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:135

Publication(s):Ebert et al. 2021

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: 709 SVs from 59 studies. See in: genome view

Submitted genomic15,048,964-15,049,098

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5592627	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	15,048,964	15,049,098
nsv5592627	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	15,142,821	15,142,955

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17081485	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17081485	Submitted genomic		NC_000016.10:g.150 48964_15049098delG	GRCh38 (hg38)		NC_000016.10	Chr16	15,048,964	15,049,098
nssv17081485	Remapped	Perfect	NC_000016.9:g.1514 2821_15142955delG	GRCh37.p13	First Pass	NC_000016.9	Chr16	15,142,821	15,142,955

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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