A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145447



Internal ID15998633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133440431..133445787hg38UCSC Ensembl
Innerchr9:136305552..136310908hg19UCSC Ensembl
Innerchr9:135295373..135300729hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385357
hg195357
hg185357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615636
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)nssv1145447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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