A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711032



Internal ID134698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5197851..5197916hg38UCSC Ensembl
chr17:5101146..5101211hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528393
Supporting Variants
Samples
Known GenesLOC100130950
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711032
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010648


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