A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520350



Internal ID15100957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4203214..4358255hg38UCSC Ensembl
Innerchr9:4203214..4358255hg19UCSC Ensembl
Innerchr9:4193214..4348255hg18UCSC Ensembl
Innerchr9:4193214..4348255hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38155042
hg19155042
hg18155042
hg17155042
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699984, nssv703731, nssv663100, nssv704738, nssv672852
Samples
Known GenesGLIS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520350
Frequency
Sample Size2026
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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