A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961256



Internal ID41478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183065032..183067381hg38UCSC Ensembl
chr4:183986185..183988534hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382350
hg192350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961256
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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