A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615622



Internal ID16056345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133422462..133426501hg38UCSC Ensembl
Innerchr9:136287582..136291621hg19UCSC Ensembl
Innerchr9:135277403..135281442hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384040
hg194040
hg184040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145409
Samples
Known GenesADAMTS13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615622
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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