A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615598



Internal ID16056321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133061291..133082065hg38UCSC Ensembl
Innerchr9:135936678..135957452hg19UCSC Ensembl
Innerchr9:134926499..134947273hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3820775
hg1920775
hg1820775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12925n54
Supporting Variantsnssv1145384, nssv1145382, nssv1145383
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615598
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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