A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713775



Internal ID137441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57795156..57795276hg38UCSC Ensembl
chr17:55872517..55872637hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713775
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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