A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181290



Internal ID20748330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124443012..124443076hg38UCSC Ensembl
chr11:124312908..124312972hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.71035


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