A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039713



Internal ID18782244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75101872..75382048hg38UCSC Ensembl
Innerchr15:75394213..75674389hg19UCSC Ensembl
Innerchr15:73181266..73461442hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38280177
hg19280177
hg18280177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2621n100
Supporting Variantsnssv3553698
Samples
Known GenesC15orf39, COMMD4, GOLGA6C, GOLGA6D, MAN2C1, MIR631, NEIL1, SIN3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039713
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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