A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528916



Internal ID15456209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95571914..95582377hg38UCSC Ensembl
Innerchr12:95965690..95976153hg19UCSC Ensembl
Innerchr12:94489821..94500284hg18UCSC Ensembl
Innerchr12:94468158..94478621hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3810464
hg1910464
hg1810464
hg1710464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705603
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528916
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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