A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216176



Internal ID20783216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31734983..31775928hg38UCSC Ensembl
chr5:31735090..31776035hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3840946
hg1940946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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