A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519793



Internal ID296138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44305280..44314329hg38UCSC Ensembl
chr15:44597478..44606527hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg389050
hg199050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702990
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519793
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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