A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2652n100



Internal ID22788739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85796276..85807277hg38UCSC Ensembl
chr15:86339507..86350508hg19UCSC Ensembl
chr15:84140511..84151512hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3811002
hg1911002
hg1811002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041242, nsv1042097
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)dgv2652n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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