A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730626



Internal ID154292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6759097..6759100hg38UCSC Ensembl
chr20:6739744..6739747hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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