A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525662



Internal ID15452955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23412125..23426988hg38UCSC Ensembl
Innerchr11:23433671..23448534hg19UCSC Ensembl
Innerchr11:23390247..23405110hg18UCSC Ensembl
Innerchr11:23390247..23405110hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3814864
hg1914864
hg1814864
hg1714864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701818
Samples
Known GenesMIR8054
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525662
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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