A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779886



Internal ID15727156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85977166..86064017hg38UCSC Ensembl
Innerchr11:85688209..85775059hg19UCSC Ensembl
Innerchr11:85365857..85452707hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3886852
hg1986851
hg1886851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555644
Supporting Variants
Samples
Known GenesPICALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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