A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525113



Internal ID15105720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97907517..97924533hg38UCSC Ensembl
Innerchr9:100669799..100686815hg19UCSC Ensembl
Innerchr9:99709620..99726636hg18UCSC Ensembl
Innerchr9:97749354..97766370hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3817017
hg1917017
hg1817017
hg1717017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701175
Samples
Known GenesC9orf156
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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