A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525879



Internal ID15106486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55091394..55165977hg38UCSC Ensembl
Innerchr1:55557067..55631650hg19UCSC Ensembl
Innerchr1:55329655..55404238hg18UCSC Ensembl
Innerchr1:55269088..55343671hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3874584
hg1974584
hg1874584
hg1774584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702079
Samples
Known GenesUSP24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525879
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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