A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780269



Internal ID16074225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89012271..89125229hg38UCSC Ensembl
Innerchr11:88745439..88858397hg19UCSC Ensembl
Innerchr11:88385087..88498045hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38112959
hg19112959
hg18112959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555733
Supporting Variants
Samples
Known GenesGRM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv780269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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