A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893666



Internal ID19184486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:19271204..19572787hg38UCSC Ensembl
Outerchr3:19271204..19572787hg38UCSC Ensembl
Innerchr3:19312696..19614279hg19UCSC Ensembl
Outerchr3:19312696..19614279hg19UCSC Ensembl
Innerchr3:19287700..19589283hg18UCSC Ensembl
Outerchr3:19287700..19589283hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38301584
hg19301584
hg18301584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797819
Samples
Known GenesKCNH8, MIR4791
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893666
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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