A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977745



Internal ID52555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178226346..178233684hg38UCSC Ensembl
chr5:177653347..177660685hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387339
hg197339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462249
Supporting Variants
Samples
Known GenesPHYKPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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