A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949227



Internal ID33502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62088446..62092764hg38UCSC Ensembl
chr4:62954164..62958482hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg384319
hg194319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949227
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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