A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521969



Internal ID15449262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9313414..9357458hg38UCSC Ensembl
Innerchr11:9334961..9379005hg19UCSC Ensembl
Innerchr11:9291537..9335581hg18UCSC Ensembl
Innerchr11:9291537..9335581hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844045
hg1944045
hg1844045
hg1744045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694738
Samples
Known GenesTMEM41B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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