A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613945



Internal ID16401354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27121908..27148477hg38UCSC Ensembl
Innerchr9:27121906..27148475hg19UCSC Ensembl
Innerchr9:27111906..27138475hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3826570
hg1926570
hg1826570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132072
Samples
Known GenesTEK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613945
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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