A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662555



Internal ID15052521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111769091..111868361hg38UCSC Ensembl
Innerchr12:112206895..112306165hg19UCSC Ensembl
Innerchr12:110691278..110790548hg18UCSC Ensembl
Innerchr12:110669615..110768885hg17UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3899271
hg1999271
hg1899271
hg1799271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515716
Supporting Variants
Samples
Known GenesALDH2, MAPKAPK5, MAPKAPK5-AS1, MIR6761
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662555
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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