A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127748



Internal ID20694788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157706859..157711902hg38UCSC Ensembl
chr5:157133867..157138910hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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