A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126990



Internal ID20694030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152356369..152356806hg38UCSC Ensembl
chr5:151735930..151736367hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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