A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214862



Internal ID20781902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68017901..68024500hg38UCSC Ensembl
chr5:67313729..67320328hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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