A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992874



Internal ID7078207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45810702..45814282hg38UCSC Ensembl
Innerchr7:45850301..45853881hg19UCSC Ensembl
Innerchr7:45816826..45820406hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg383581
hg193581
hg183581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586074
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992874
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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