A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2653n100



Internal ID22788740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85796276..85813084hg38UCSC Ensembl
chr15:86339507..86356315hg19UCSC Ensembl
chr15:84140511..84157319hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3816809
hg1916809
hg1816809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045565, nsv1049241, nsv1052174
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)dgv2653n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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