A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509528



Internal ID286179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43282345..43292265hg38UCSC Ensembl
chr15:43574543..43584463hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg389921
hg199921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702004
Samples
Known GenesTGM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509528
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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