A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509336



Internal ID285994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34073843..34078844hg38UCSC Ensembl
chr15:34366044..34371045hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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