A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714017



Internal ID137683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63705749..63705885hg38UCSC Ensembl
chr17:61783109..61783245hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523089
Supporting Variants
Samples
Known GenesSTRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714017
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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