A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214093



Internal ID20781133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64689201..64695400hg38UCSC Ensembl
chr5:63985028..63991227hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415056
Supporting Variants
Samples
Known GenesFAM159B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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