A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905702



Internal ID4609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80492666..80501630hg38UCSC Ensembl
chr1:80958351..80967315hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg388965
hg198965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905702
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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