A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035327



Internal ID91289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77851718..77851843hg38UCSC Ensembl
chr10:79611476..79611601hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488497
Supporting Variants
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035327
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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