A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005705



Internal ID6717825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79711655..79732597hg38UCSC Ensembl
Innerchr10:81471411..81492353hg19UCSC Ensembl
Innerchr10:81141417..81162359hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3820943
hg1920943
hg1820943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586057
SamplesHuRef
Known GenesNUTM2B
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005705
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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