A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560507



Internal ID333514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10298268..10303401hg38UCSC Ensembl
chr8:10155778..10160911hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385134
hg195134
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007373
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560507
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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