A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892484



Internal ID19183304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26907693..27016468hg38UCSC Ensembl
Outerchr14:26907693..27016468hg38UCSC Ensembl
Innerchr14:27376899..27485674hg19UCSC Ensembl
Outerchr14:27376899..27485674hg19UCSC Ensembl
Innerchr14:26446739..26555514hg18UCSC Ensembl
Outerchr14:26446739..26555514hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38108776
hg19108776
hg18108776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798111, essv25798088
Samples
Known GenesMIR4307
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892484
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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