A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994034



Internal ID7062829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39741152..39879297hg38UCSC Ensembl
Innerchr9:41886170..42024315hg19UCSC Ensembl
Innerchr9:41876170..42014315hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38138146
hg19138146
hg18138146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586692
SamplesHuRef
Known GenesKGFLP2, LOC643648, MGC21881
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994034
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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