A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893661



Internal ID19184481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8597882..8680359hg38UCSC Ensembl
Outerchr3:8597882..8680359hg38UCSC Ensembl
Innerchr3:8639568..8722045hg19UCSC Ensembl
Outerchr3:8639568..8722045hg19UCSC Ensembl
Innerchr3:8614568..8697045hg18UCSC Ensembl
Outerchr3:8614568..8697045hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3882478
hg1982478
hg1882478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799806
Samples
Known GenesSSUH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893661
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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