A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015178



Internal ID77773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109085100..109086998hg38UCSC Ensembl
chr8:110097329..110099227hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015178
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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