A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892629



Internal ID18836763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20792030..20932790hg38UCSC Ensembl
Outerchr15:20792030..20932790hg38UCSC Ensembl
Innerchr15:20997359..21138119hg19UCSC Ensembl
Outerchr15:20997359..21138119hg19UCSC Ensembl
Innerchr15:19257404..19402778hg18UCSC Ensembl
Outerchr15:19257404..19402778hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38140761
hg19140761
hg18145375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797907
Samples
Known GenesCXADRP2, NF1P2, POTEB, POTEB2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892629
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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