A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726007



Internal ID149673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43608141..43608265hg38UCSC Ensembl
chr20:42236781..42236905hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528687
Supporting Variants
Samples
Known GenesIFT52
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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