A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711097



Internal ID134763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6163038..6163109hg38UCSC Ensembl
chr17:6066358..6066429hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711097
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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