A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661013



Internal ID15397665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7832345..7905327hg38UCSC Ensembl
Innerchr12:7984941..8057923hg19UCSC Ensembl
Innerchr12:7876208..7949190hg18UCSC Ensembl
Innerchr12:7876208..7949190hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3872983
hg1972983
hg1872983
hg1772983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516107
Supporting Variants
Samples
Known GenesSLC2A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661013
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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