A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790819



Internal ID18816656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7587317..7999743hg38UCSC Ensembl
Innerchr20:7567964..7980390hg19UCSC Ensembl
Innerchr20:7515964..7928390hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38412427
hg19412427
hg18412427
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893279
Supporting Variants
Samples
Known GenesHAO1, TMX4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=106
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790819
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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