A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013296



Internal ID76539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78344173..78358875hg38UCSC Ensembl
chr8:79256408..79271110hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3814703
hg1914703
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013296
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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