A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442603



Internal ID221025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209359257..209359336hg38UCSC Ensembl
chr1:209532602..209532681hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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