A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798686



Internal ID18822975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30389978hg38UCSC Ensembl
Innerchr15:30487045..30682181hg19UCSC Ensembl
Innerchr15:28274337..28469473hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38195137
hg19195137
hg18195137
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892642
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=48
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798686
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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