A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524109



Internal ID15451402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126732558..126735139hg38UCSC Ensembl
Innerchr11:126602453..126605034hg19UCSC Ensembl
Innerchr11:126107663..126110244hg18UCSC Ensembl
Innerchr11:126107663..126110244hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382582
hg192582
hg182582
hg172582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699987
Samples
Known GenesKIRREL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524109
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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