A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702693



Internal ID126359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51527913..51528836hg38UCSC Ensembl
chr15:51820110..51821033hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522376
Supporting Variants
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702693
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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