A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613618



Internal ID16401027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13309614..13339622hg38UCSC Ensembl
Innerchr9:13309613..13339621hg19UCSC Ensembl
Innerchr9:13299613..13329621hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3830009
hg1930009
hg1830009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128719, nssv1128720
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613618
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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