A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010035



Internal ID74330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26872678..26899150hg38UCSC Ensembl
chr8:26730195..26756667hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3826473
hg1926473
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010035
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003746


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