A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528022



Internal ID15455315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21969441..22071287hg38UCSC Ensembl
Innerchr11:21990987..22092833hg19UCSC Ensembl
Innerchr11:21947563..22049409hg18UCSC Ensembl
Innerchr11:21947563..22049409hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38101847
hg19101847
hg18101847
hg17101847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704551
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528022
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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