A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961255



Internal ID41477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183059131..183059206hg38UCSC Ensembl
chr4:183980284..183980359hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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