A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586215



Internal ID21778258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113444336..113444388hg38UCSC Ensembl
chr8:114456565..114456617hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586215
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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