A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905721



Internal ID4619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80584945..80602377hg38UCSC Ensembl
chr1:81050630..81068062hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3817433
hg1917433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905721
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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