A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513982



Internal ID290487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53682263..53684817hg38UCSC Ensembl
chr15:53974460..53977014hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382555
hg192555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701247
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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