A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005872



Internal ID7070966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66181139..66208547hg38UCSC Ensembl
Innerchr9:70707924..70735468hg19UCSC Ensembl
Innerchr9:69947744..69975288hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3827409
hg1927545
hg1827545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586554
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005872
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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