A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486734



Internal ID264092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30794490..30871768hg38UCSC Ensembl
chr9:30794488..30871766hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3877279
hg1977279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486734
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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