A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907277



Internal ID5638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5117360..5123510hg38UCSC Ensembl
chr1:5177420..5183570hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg386151
hg196151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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