A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520167



Internal ID21844526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89200185..89200250hg38UCSC Ensembl
chr1:89665868..89665933hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520167
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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