A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955786



Internal ID37827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:130115828..130127482hg38UCSC Ensembl
chr4:131036983..131048637hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3811655
hg1911655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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