A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789488



Internal ID18833200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72255497..72756402hg38UCSC Ensembl
Innerchr14:72722205..73223110hg19UCSC Ensembl
Innerchr14:71791958..72292863hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38500906
hg19500906
hg18500906
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892558
Supporting Variants
Samples
Known GenesDPF3, MIR7843, RGS6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=161
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789488
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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