A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2627n100



Internal ID22788714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76562864..76603422hg38UCSC Ensembl
chr15:76855205..76895763hg19UCSC Ensembl
chr15:74642260..74682818hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3840559
hg1940559
hg1840559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044453, nsv1037282, nsv1038233
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2627n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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