A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891580



Internal ID168579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166756263..166765412hg38UCSC Ensembl
chr1:166725500..166734649hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg389150
hg199150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891580
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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