A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv769276



Internal ID16063232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26829145..26883949hg38UCSC Ensembl
Innerchr11:26850692..26905496hg19UCSC Ensembl
Innerchr11:26807268..26862072hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3854805
hg1954805
hg1854805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553911
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv769276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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