A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893669



Internal ID18837803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20001342..20074585hg38UCSC Ensembl
Outerchr3:20001342..20074585hg38UCSC Ensembl
Innerchr3:20042834..20116077hg19UCSC Ensembl
Outerchr3:20042834..20116077hg19UCSC Ensembl
Innerchr3:20017838..20091081hg18UCSC Ensembl
Outerchr3:20017838..20091081hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3873244
hg1973244
hg1873244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782843
Samples
Known GenesKAT2B, PP2D1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893669
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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