A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614145



Internal ID16054868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32873874..32930290hg38UCSC Ensembl
Innerchr9:32873872..32930288hg19UCSC Ensembl
Innerchr9:32863872..32920288hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3856417
hg1956417
hg1856417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132838
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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