A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2976561



Internal ID15652163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:514394..526664hg38UCSC Ensembl
Innerchr9:514394..526664hg19UCSC Ensembl
Innerchr9:504394..516664hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3812271
hg1912271
hg1812271
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515144
Supporting Variants
SamplesNA12818
Known GenesKANK1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2976561
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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