A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479461



Internal ID256985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134078305..134081869hg38UCSC Ensembl
chr9:136943427..136946991hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383565
hg193565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479461
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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