A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615632



Internal ID16403041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133429017..133429735hg38UCSC Ensembl
Innerchr9:136294137..136294855hg19UCSC Ensembl
Innerchr9:135283958..135284676hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38719
hg19719
hg18719
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12936n54
Supporting Variantsnssv1145434, nssv1145435
Samples
Known GenesADAMTS13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615632
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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