A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2647n100



Internal ID20154263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85268380..85470404hg38UCSC Ensembl
chr15:85811611..86013635hg19UCSC Ensembl
chr15:83612615..83814639hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38202025
hg19202025
hg18202025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046337, nsv1039043
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)dgv2647n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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