A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2621n100



Internal ID20154237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75101872..75382048hg38UCSC Ensembl
chr15:75394213..75674389hg19UCSC Ensembl
chr15:73181266..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 Variants
Supporting Variantsnsv1039713, nsv1037713
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)dgv2621n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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