A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522376



Internal ID298647
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 StatusM
Merged Variants
Supporting Variantsnssv17702693
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522376
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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