A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001418



Internal ID7066544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62369925..62632384hg38UCSC Ensembl
Innerchr9:46681226..46943685hg19UCSC Ensembl
Innerchr9:46521222..46783505hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg38262460
hg19262460
hg18262284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586321
SamplesHuRef
Known GenesKGFLP1, LOC643648
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001418
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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