A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524728



Internal ID15105335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43538441..43554216hg38UCSC Ensembl
Innerchr11:43559991..43575766hg19UCSC Ensembl
Innerchr11:43516567..43532342hg18UCSC Ensembl
Innerchr11:43516567..43532342hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3815776
hg1915776
hg1815776
hg1715776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv66n21
Supporting Variantsnssv700717
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524728
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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