A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906481



Internal ID5114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92427409..92435807hg38UCSC Ensembl
chr1:92892966..92901364hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg388399
hg198399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906481
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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