A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527566



Internal ID15454859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95833355..95844816hg38UCSC Ensembl
Innerchr13:96485609..96497070hg19UCSC Ensembl
Innerchr13:95283610..95295071hg18UCSC Ensembl
Innerchr13:95283610..95295071hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3811462
hg1911462
hg1811462
hg1711462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704027
Samples
Known GenesUGGT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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