A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613133



Internal ID16053856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2403909..2421273hg38UCSC Ensembl
Innerchr9:2403909..2421273hg19UCSC Ensembl
Innerchr9:2393909..2411273hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3817365
hg1917365
hg1817365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156437
SamplesNINDS_134
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613133
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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