A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134278



Internal ID20701318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89898681..89899273hg38UCSC Ensembl
chr5:89194498..89195090hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134278
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00062


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