A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2585n100



Internal ID22788672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43600874..43703678hg38UCSC Ensembl
chr15:43893072..43995876hg19UCSC Ensembl
chr15:41680364..41783168hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38102805
hg19102805
hg18102805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047829, nsv1053621, nsv1036941, nsv1037061
Samples
Known GenesCATSPER2, CKMT1A, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2585n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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