A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521936



Internal ID15102543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125200496..125214846hg38UCSC Ensembl
Innerchr11:125070392..125084742hg19UCSC Ensembl
Innerchr11:124575602..124589952hg18UCSC Ensembl
Innerchr11:124575602..124589952hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814351
hg1914351
hg1814351
hg1714351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv83n21
Supporting Variantsnssv694705
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521936
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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