A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525618



Internal ID18823899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113081728..113611496hg38UCSC Ensembl
Innerchr13:113736042..114265811hg19UCSC Ensembl
Innerchr13:112784043..113313812hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38529769
hg19529770
hg18529770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048814
Supporting Variants
Samples
Known GenesADPRHL1, CUL4A, DCUN1D2, F10, F7, GRTP1, LAMP1, MCF2L, MIR8075, PCID2, PROZ, TFDP1, TMCO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525618
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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