A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179931



Internal ID20746971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123137228..123142757hg38UCSC Ensembl
chr11:123007936..123013465hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385530
hg195530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462314
Supporting Variants
Samples
Known GenesCLMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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