A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010786



Internal ID74819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61742167..61801446hg38UCSC Ensembl
chr8:62654726..62714005hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3859280
hg1959280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010786
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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