A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426373



Internal ID22484243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159766491..159766703hg38UCSC Ensembl
chr5:159193498..159193710hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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