A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893751



Internal ID19184571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99047482..99080755hg38UCSC Ensembl
Outerchr3:99047482..99080755hg38UCSC Ensembl
Innerchr3:98766326..98799599hg19UCSC Ensembl
Outerchr3:98766326..98799599hg19UCSC Ensembl
Innerchr3:100249016..100282289hg18UCSC Ensembl
Outerchr3:100249016..100282289hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3833274
hg1933274
hg1833274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797465
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893751
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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