A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954483



Internal ID36979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120410800..120414431hg38UCSC Ensembl
chr4:121331955..121335586hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg383632
hg193632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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