A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735132



Internal ID158798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87917949..87922174hg38UCSC Ensembl
chr4:88839101..88843326hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384226
hg194226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735132
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003279


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