A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701366



Internal ID125032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55484288..55490777hg38UCSC Ensembl
chr15:55776486..55782975hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386490
hg196490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530089
Supporting Variants
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701366
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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