A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614158



Internal ID16401567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34957616..34958470hg38UCSC Ensembl
Innerchr9:34957613..34958467hg19UCSC Ensembl
Innerchr9:34947613..34948467hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38855
hg19855
hg18855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12660n54
Supporting Variantsnssv1132850
Samples
Known GenesKIAA1045
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614158
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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