A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432280



Internal ID211028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54112661..54128406hg38UCSC Ensembl
chr1:54578334..54594079hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3815746
hg1915746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432280
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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