A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719680



Internal ID143346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77092593..77092721hg38UCSC Ensembl
chr18:74804549..74804677hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531031
Supporting Variants
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719680
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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