A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779222



Internal ID15726492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76643071..76672762hg38UCSC Ensembl
Innerchr11:76354115..76383806hg19UCSC Ensembl
Innerchr11:76031763..76061454hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3829692
hg1929692
hg1829692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555448
Supporting Variants
Samples
Known GenesLRRC32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779222
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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