A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518592



Internal ID15099199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61481911..61487543hg38UCSC Ensembl
Innerchr11:61249383..61255015hg19UCSC Ensembl
Innerchr11:61005959..61011591hg18UCSC Ensembl
Innerchr11:61005959..61011591hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385633
hg195633
hg185633
hg175633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696039
Samples
Known GenesPPP1R32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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