A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966155



Internal ID44752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67041726..67042273hg38UCSC Ensembl
chr5:66337554..66338101hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456085
Supporting Variants
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966155
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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