A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522229



Internal ID15449522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15919553..15925257hg38UCSC Ensembl
Innerchr11:15941099..15946803hg19UCSC Ensembl
Innerchr11:15897675..15903379hg18UCSC Ensembl
Innerchr11:15897675..15903379hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385705
hg195705
hg185705
hg175705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694146
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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