A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524777



Internal ID15105384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11883811..11897151hg38UCSC Ensembl
Innerchr11:11905358..11918698hg19UCSC Ensembl
Innerchr11:11861934..11875274hg18UCSC Ensembl
Innerchr11:11861934..11875274hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813341
hg1913341
hg1813341
hg1713341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700768
Samples
Known GenesUSP47
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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