A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214841



Internal ID20781881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66097024..66131648hg38UCSC Ensembl
chr5:65392852..65427476hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3834625
hg1934625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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