A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994970



Internal ID7079505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:358323..382608hg38UCSC Ensembl
Innerchr1:436729..461014hg19UCSC Ensembl
Innerchr1:426592..450877hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3824286
hg1924286
hg1824286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586250
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994970
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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