A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520100



Internal ID296440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72735139..72735279hg38UCSC Ensembl
chr15:73027480..73027620hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702448
Samples
Known GenesBBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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