A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2596n100



Internal ID22788683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52698270..52749690hg38UCSC Ensembl
chr15:52990467..53041887hg19UCSC Ensembl
chr15:50777759..50829179hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3851421
hg1951421
hg1851421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049619, nsv1035212, nsv1049144, nsv1049055
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2596n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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