A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560201



Internal ID333214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47257037..47308898hg38UCSC Ensembl
chr3:47298527..47350388hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3851862
hg1951862
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932018
Samples
Known GenesKIF9, KLHL18
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560201
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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