A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790252



Internal ID18819091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185291669..185483550hg38UCSC Ensembl
Innerchr3:185009457..185201338hg19UCSC Ensembl
Innerchr3:186492151..186684032hg18UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38191882
hg19191882
hg18191882
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893837
Supporting Variants
Samples
Known GenesMAP3K13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790252
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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