A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893718



Internal ID19184538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67266860..67294799hg38UCSC Ensembl
Outerchr3:67266860..67294799hg38UCSC Ensembl
Innerchr3:67317284..67345223hg19UCSC Ensembl
Outerchr3:67317284..67345223hg19UCSC Ensembl
Innerchr3:67399974..67427913hg18UCSC Ensembl
Outerchr3:67399974..67427913hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3827940
hg1927940
hg1827940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796603
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893718
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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