A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145420



Internal ID15998606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133428911..133429576hg38UCSC Ensembl
Innerchr9:136294031..136294696hg19UCSC Ensembl
Innerchr9:135283852..135284517hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38666
hg19666
hg18666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615627
Supporting Variants
Samples
Known GenesADAMTS13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145420
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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