A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521541



Internal ID15448834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31744146..31754035hg38UCSC Ensembl
Innerchr14:32213352..32223241hg19UCSC Ensembl
Innerchr14:31283103..31292992hg18UCSC Ensembl
Innerchr14:31283103..31292992hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg389890
hg199890
hg189890
hg179890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698157
Samples
Known GenesNUBPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521541
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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