A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010714



Internal ID7074665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:5669705..5675621hg38UCSC Ensembl
Innerchr12:5778871..5784787hg19UCSC Ensembl
Innerchr12:5649132..5655048hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg385917
hg195917
hg185917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586854
SamplesHuRef
Known GenesANO2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010714
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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