A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553372



Internal ID15994095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6489014..6529079hg38UCSC Ensembl
Innerchr11:6510244..6550309hg19UCSC Ensembl
Innerchr11:6466820..6506885hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3840066
hg1940066
hg1840066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766329
Samples
Known GenesDNHD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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