A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555453



Internal ID15996176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77866448..77907395hg38UCSC Ensembl
Innerchr11:77577494..77618441hg19UCSC Ensembl
Innerchr11:77255142..77296089hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3840948
hg1940948
hg1840948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779226
Samples
Known GenesAAMDC, INTS4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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