A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479073



Internal ID256611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106038640..106044587hg38UCSC Ensembl
chr9:108800921..108806868hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385948
hg195948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479073
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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