A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526785



Internal ID15454078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88247298..88251932hg38UCSC Ensembl
Innerchr11:87980466..87985100hg19UCSC Ensembl
Innerchr11:87620114..87624748hg18UCSC Ensembl
Innerchr11:87620114..87624748hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg384635
hg194635
hg184635
hg174635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv76n21
Supporting Variantsnssv703137
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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