A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784643



Internal ID15731913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122837181..122863109hg38UCSC Ensembl
Innerchr11:122707889..122733817hg19UCSC Ensembl
Innerchr11:122213099..122239027hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3825929
hg1925929
hg1825929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556481
Supporting Variants
Samples
Known GenesCRTAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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