A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520872



Internal ID15448165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58976211..59102985hg38UCSC Ensembl
Innerchr15:59268410..59395184hg19UCSC Ensembl
Innerchr15:57055702..57182476hg18UCSC Ensembl
Innerchr15:57055702..57182476hg17UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38126775
hg19126775
hg18126775
hg17126775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv151n21
Supporting Variantsnssv697660
Samples
Known GenesRNF111
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520872
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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