A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996134



Internal ID6732078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42628776..42630987hg38UCSC Ensembl
Innerchr5:42628878..42631089hg19UCSC Ensembl
Innerchr5:42664635..42666846hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382212
hg192212
hg182212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv143e180
Supporting Variantsessv3586904
SamplesHuRef
Known GenesGHR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996134
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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