A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955630



Internal ID37729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110439075..110439242hg38UCSC Ensembl
chr4:111360231..111360398hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463602
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955630
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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