A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522551



Internal ID15449844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81706078..81842113hg38UCSC Ensembl
Innerchr11:81417120..81553155hg19UCSC Ensembl
Innerchr11:81094768..81230803hg18UCSC Ensembl
Innerchr11:81094768..81230803hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38136036
hg19136036
hg18136036
hg17136036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705932
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522551
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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