A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614559



Internal ID16055282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126657..69127886hg38UCSC Ensembl
Innerchr9:71741573..71742802hg19UCSC Ensembl
Innerchr9:70931393..70932622hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381230
hg191230
hg181230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12741n54
Supporting Variantsnssv1135819
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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