A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615466



Internal ID16402875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129453264..129471535hg38UCSC Ensembl
Innerchr9:132215543..132233814hg19UCSC Ensembl
Innerchr9:131255364..131273635hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818272
hg1918272
hg1818272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12902n54
Supporting Variantsnssv1145031
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615466
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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