A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523952



Internal ID15104559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45961834..46006730hg38UCSC Ensembl
Innerchr11:45983385..46028281hg19UCSC Ensembl
Innerchr11:45939961..45984857hg18UCSC Ensembl
Innerchr11:45939961..45984857hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3844897
hg1944897
hg1844897
hg1744897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699800
Samples
Known GenesPHF21A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523952
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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