A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126834



Internal ID20693874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158618101..158625100hg38UCSC Ensembl
chr5:158045109..158052108hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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