A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782843



Internal ID18812937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20001342..20074585hg38UCSC Ensembl
Innerchr3:20042834..20116077hg19UCSC Ensembl
Innerchr3:20017838..20091081hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3873244
hg1973244
hg1873244
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893669
Supporting Variants
Samples
Known GenesKAT2B, PP2D1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782843
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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