A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892582



Internal ID18836716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103788746..103866422hg38UCSC Ensembl
Outerchr14:103788746..103866422hg38UCSC Ensembl
Innerchr14:104255083..104332759hg19UCSC Ensembl
Outerchr14:104255083..104332759hg19UCSC Ensembl
Innerchr14:103324836..103402512hg18UCSC Ensembl
Outerchr14:103324836..103402512hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3877677
hg1977677
hg1877677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784905
Samples
Known GenesLINC00637, PPP1R13B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892582
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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