A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2603n100



Internal ID22788690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54836089..54890626hg38UCSC Ensembl
chr15:55128287..55182824hg19UCSC Ensembl
chr15:52915579..52970116hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3854538
hg1954538
hg1854538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039749, nsv1036047
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)dgv2603n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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