A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2626n100



Internal ID22788713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76168121..76193625hg38UCSC Ensembl
chr15:76460462..76485966hg19UCSC Ensembl
chr15:74247517..74273021hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3825505
hg1925505
hg1825505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053775, nsv1046563
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2626n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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