A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896005



Internal ID171489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223374175..223374237hg38UCSC Ensembl
chr1:223547517..223547579hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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