A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892558



Internal ID18836692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72255497..72756402hg38UCSC Ensembl
Outerchr14:72255497..72756402hg38UCSC Ensembl
Innerchr14:72722205..73223110hg19UCSC Ensembl
Outerchr14:72722205..73223110hg19UCSC Ensembl
Innerchr14:71791958..72292863hg18UCSC Ensembl
Outerchr14:71791958..72292863hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38500906
hg19500906
hg18500906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789488
Samples
Known GenesDPF3, MIR7843, RGS6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892558
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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