A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703731



Internal ID15093697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4262516..4272449hg38UCSC Ensembl
Innerchr9:4262516..4272449hg19UCSC Ensembl
Innerchr9:4252516..4262449hg18UCSC Ensembl
Innerchr9:4252516..4262449hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg389934
hg199934
hg189934
hg179934
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv703731
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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