A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216814



Internal ID20783854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111074401..111078918hg38UCSC Ensembl
chr6:111395604..111400121hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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