A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010685



Internal ID74754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38535851..38537607hg38UCSC Ensembl
chr8:38393369..38395125hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381757
hg191757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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