A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186267



Internal ID20753308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69911904..69925788hg38UCSC Ensembl
chr11_gl000202_random:9157..23225hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813885
hg1914069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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