A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522838



Internal ID15450131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96528892..96608086hg38UCSC Ensembl
Innerchr9:99291174..99370368hg19UCSC Ensembl
Innerchr9:98330995..98410189hg18UCSC Ensembl
Innerchr9:96370729..96449923hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3879195
hg1979195
hg1879195
hg1779195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698490
Samples
Known GenesCDC14B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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