A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2648n100



Internal ID22788735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85268380..85605207hg38UCSC Ensembl
chr15:85811611..86148438hg19UCSC Ensembl
chr15:83612615..83949442hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38336828
hg19336828
hg18336828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037963, nsv1040998, nsv1050679, nsv1048308, nsv1052259, nsv1037765, nsv1037988, nsv1046189, nsv1049705
Samples
Known GenesAKAP13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2648n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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