A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148381



Internal ID16001567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138131866..138214775hg38UCSC Ensembl
Innerchr9:141026318..141105225hg19UCSC Ensembl
Innerchr9:140146139..140225046hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3882910
hg1978908
hg1878908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616028
Supporting Variants
Samples
Known GenesTUBBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148381
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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