A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523150



Internal ID18474745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22950543..24316879hg38UCSC Ensembl
Innerchr13:23524682..24891017hg19UCSC Ensembl
Innerchr13:22422682..23789017hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381366337
hg191366336
hg181366336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044362
Supporting Variants
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523150
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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