A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900291



Internal ID986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28346123..28351512hg38UCSC Ensembl
chr1:28672634..28678023hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg385390
hg195390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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