A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001895



Internal ID7067013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2208330..2211252hg38UCSC Ensembl
Innerchr5:2208444..2211366hg19UCSC Ensembl
Innerchr5:2261444..2264366hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382923
hg192923
hg182923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587024
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001895
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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