A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125531



Internal ID20692571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122540233..122540871hg38UCSC Ensembl
chr5:121875928..121876566hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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