A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715093



Internal ID138759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83180066..83219133hg38UCSC Ensembl
chr17:81127835..81166902hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3839068
hg1939068
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002355


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