A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796550



Internal ID18834826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43623873..43698012hg38UCSC Ensembl
Innerchr15:43916071..43990210hg19UCSC Ensembl
Innerchr15:41703363..41777502hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3874140
hg1974140
hg1874140
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892683
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796550
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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