A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992503



Internal ID6728465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:586078..612499hg38UCSC Ensembl
Innerchr1:521458..547879hg19UCSC Ensembl
Innerchr1:511321..537742hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3826422
hg1926422
hg1826422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586722
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992503
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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