A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524282



Internal ID15451575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97914884..97922475hg38UCSC Ensembl
Innerchr9:100677166..100684757hg19UCSC Ensembl
Innerchr9:99716987..99724578hg18UCSC Ensembl
Innerchr9:97756721..97764312hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg387592
hg197592
hg187592
hg177592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700181
Samples
Known GenesC9orf156
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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