A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787985



Internal ID19172924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73561413..73610781hg38UCSC Ensembl
Innerchr14:74028117..74077485hg19UCSC Ensembl
Innerchr14:73097870..73147238hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3849369
hg1949369
hg1849369
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892562
Supporting Variants
Samples
Known GenesACOT2, ACOT4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787985
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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