A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527782



Internal ID15108389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8604195..8604885hg38UCSC Ensembl
Innerchr12:8756791..8757481hg19UCSC Ensembl
Innerchr12:8648058..8648748hg18UCSC Ensembl
Innerchr12:8648058..8648748hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38691
hg19691
hg18691
hg17691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704273
Samples
Known GenesAICDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527782
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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