A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480399



Internal ID257907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20002304..20034512hg38UCSC Ensembl
chr10:20291233..20323441hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3832209
hg1932209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032150
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480399
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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