A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699339



Internal ID15089305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125302697..125302778hg38UCSC Ensembl
Innerchr11:125172593..125172674hg19UCSC Ensembl
Innerchr11:124677803..124677884hg18UCSC Ensembl
Innerchr11:124677803..124677884hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3882
hg1982
hg1882
hg1782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523559
Supporting Variants
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699339
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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