A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672852



Internal ID15062818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4206388..4358255hg38UCSC Ensembl
Innerchr9:4206388..4358255hg19UCSC Ensembl
Innerchr9:4196388..4348255hg18UCSC Ensembl
Innerchr9:4196388..4348255hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38151868
hg19151868
hg18151868
hg17151868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520350
Supporting Variants
Samples
Known GenesGLIS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672852
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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