A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478220



Internal ID255782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120475019..120476709hg38UCSC Ensembl
chr8:121487259..121488949hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016021
Samples
Known GenesMTBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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