A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508789



Internal ID285470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102804498..102807265hg38UCSC Ensembl
chr10:104564255..104567022hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382768
hg192768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039961
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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