A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904229



Internal ID3637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69530711..69537019hg38UCSC Ensembl
chr1:69996394..70002702hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg386309
hg196309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904229
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011555


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