A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525224



Internal ID301396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45768191..45970247hg38UCSC Ensembl
chr15:46060389..46262445hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38202057
hg19202057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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