A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966120



Internal ID44728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66661861..66745281hg38UCSC Ensembl
chr5:65957689..66041109hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3883421
hg1983421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467789
Supporting Variants
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966120
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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