A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520683



Internal ID297002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72125514..72126938hg38UCSC Ensembl
chr15:72417855..72419279hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702420
Samples
Known GenesSENP8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520683
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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