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dbVar

Database of genomic structural variation

nsv4706811

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:307,551

Publication(s):Mwapagha 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: 1113 SVs from 76 studies. See in: genome view

Remapped(Score: Perfect):25,174,967-25,482,517

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4706811	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	25,174,967	25,482,517
nsv4706811	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	25,327,901	25,635,451

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16236135	copy number variation	M456	Sequencing	Paired-end mapping	3	4,735

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16236135	Remapped	Perfect	GRCh38.p12	First Pass	NC_000012.12	Chr12	25,174,967	25,482,517
nssv16236135	Submitted genomic		GRCh37 (hg19)		NC_000012.11	Chr12	25,327,901	25,635,451

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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