A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486238



Internal ID263607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101495208..101502990hg38UCSC Ensembl
chr9:104257490..104265272hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg387783
hg197783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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