A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525898



Internal ID15453191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12081404..12108466hg38UCSC Ensembl
Innerchr1:12141461..12168523hg19UCSC Ensembl
Innerchr1:12064048..12091110hg18UCSC Ensembl
Innerchr1:12075727..12102789hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3827063
hg1927063
hg1827063
hg1727063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702102
Samples
Known GenesTNFRSF8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525898
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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