A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530181



Internal ID306175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45251068..45251126hg38UCSC Ensembl
chr15:45543266..45543324hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530181
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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