A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800887



Internal ID18830824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34515668hg38UCSC Ensembl
Innerchr15:34730758..34807869hg19UCSC Ensembl
Innerchr15:32518050..32595161hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3877112
hg1977112
hg1877112
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892663
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800887
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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