A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432055



Internal ID22489925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42684587..42685622hg38UCSC Ensembl
chr8:42539730..42540765hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432055
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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