A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520580



Internal ID15101187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45146339..45165151hg38UCSC Ensembl
Innerchr15:45438537..45457349hg19UCSC Ensembl
Innerchr15:43225829..43244641hg18UCSC Ensembl
Innerchr15:43225829..43244641hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3818813
hg1918813
hg1818813
hg1718813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691819, nssv672790, nssv680288, nssv690520, nssv701619
Samples
Known GenesDUOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520580
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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