A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895290



Internal ID171038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206135432..206141440hg38UCSC Ensembl
chr1:206199890..206205898hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386009
hg196009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895290
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02829


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