A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949733



Internal ID33827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43456703..43456774hg38UCSC Ensembl
chr4:43458720..43458791hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949733
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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