A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715075



Internal ID138741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83122107..83197305hg38UCSC Ensembl
chr17:81075743..81145074hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3875199
hg1969332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715075
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002498


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