A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735189



Internal ID158855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147558253..147558340hg38UCSC Ensembl
chr4:148479405..148479492hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735189
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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