A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797016



Internal ID18819748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43601620..43630820hg38UCSC Ensembl
Innerchr15:43893818..43923018hg19UCSC Ensembl
Innerchr15:41681110..41710310hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3829201
hg1929201
hg1829201
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892682
Supporting Variants
Samples
Known GenesCATSPER2, RNU6-28P, STRC
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797016
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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