A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586722



Internal ID6711418
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992503
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586722
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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