A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951234



Internal ID34850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58277277..58285626hg38UCSC Ensembl
chr4:59143443..59151792hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg388350
hg198350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951234
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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