A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955616



Internal ID37717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110279046..110283552hg38UCSC Ensembl
chr4:111200202..111204708hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384507
hg194507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955616
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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