A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951204



Internal ID34832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58010219..58026245hg38UCSC Ensembl
chr4:58876385..58892411hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3816027
hg1916027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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