A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892565



Internal ID18836699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82662432..82847428hg38UCSC Ensembl
Outerchr14:82662432..82847428hg38UCSC Ensembl
Innerchr14:83128776..83313772hg19UCSC Ensembl
Outerchr14:83128776..83313772hg19UCSC Ensembl
Innerchr14:82198529..82383525hg18UCSC Ensembl
Outerchr14:82198529..82383525hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38184997
hg19184997
hg18184997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791628
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892565
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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