A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962787



Internal ID42514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19525338..19525411hg38UCSC Ensembl
chr5:19525447..19525520hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468032
Supporting Variants
Samples
Known GenesCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003122


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