A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528454



Internal ID15455747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126185145..126186619hg38UCSC Ensembl
Innerchr11:126055040..126056514hg19UCSC Ensembl
Innerchr11:125560250..125561724hg18UCSC Ensembl
Innerchr11:125560250..125561724hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381475
hg191475
hg181475
hg171475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705053
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528454
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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