A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587125



Internal ID6711821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269490..25337223hg38UCSC Ensembl
Innerchr1:25595981..25663714hg19UCSC Ensembl
Innerchr1:25468568..25536301hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3867734
hg1967734
hg1867734
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990723
Supporting Variants
SamplesHuRef
Known GenesRHD
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587125
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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