A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515121



Internal ID15466755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112620947..112823547hg38UCSC Ensembl
Innerchr9:115383227..115585827hg19UCSC Ensembl
Innerchr9:114423048..114625648hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38202601
hg19202601
hg18202601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2969268, nssv2969261, nssv2969264, nssv2969267, nssv2969265, nssv2969262, nssv2969266, nssv2969259, nssv2969260, nssv2969263
SamplesNA21438, NA19209, NA19210, NA19211, NA21523, NA21439, NA18867, NA21366, NA19204, NA21365
Known GenesINIP, KIAA1958, SNX30
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515121
Frequency
Sample Size2366
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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