A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613149



Internal ID16400558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3967758..3985549hg38UCSC Ensembl
Innerchr9:3967758..3985549hg19UCSC Ensembl
Innerchr9:3957758..3975549hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3817792
hg1917792
hg1817792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126228
Samples
Known GenesGLIS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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