A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713323



Internal ID18664918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112437023..113055517hg38UCSC Ensembl
Innerchr13:113091337..113709831hg19UCSC Ensembl
Innerchr13:112139338..112757832hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38618495
hg19618495
hg18618495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044644
Supporting Variants
Samples
Known GenesATP11A, C13orf35, MCF2L, MCF2L-AS1, TUBGCP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713323
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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