A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966676



Internal ID45103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67462538..67462603hg38UCSC Ensembl
chr5:66758366..66758431hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966676
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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