A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510390



Internal ID287011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119184563..119192600hg38UCSC Ensembl
chr10:120944075..120952112hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg388038
hg198038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n206
Supporting Variantsnssv17040869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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