A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704316



Internal ID127982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65986999..65987237hg38UCSC Ensembl
chr15:66279337..66279575hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522379
Supporting Variants
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704316
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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