A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968101



Internal ID46044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85458489..85458580hg38UCSC Ensembl
chr5:84754307..84754398hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002812


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