A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967367



Internal ID45551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69063063..69063297hg38UCSC Ensembl
chr5:68358890..68359124hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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