A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614160



Internal ID16401569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34957866..34958521hg38UCSC Ensembl
Innerchr9:34957863..34958518hg19UCSC Ensembl
Innerchr9:34947863..34948518hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38656
hg19656
hg18656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12660n54
Supporting Variantsnssv1132853, nssv1132852
Samples
Known GenesKIAA1045
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614160
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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