A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492065



Internal ID269287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65910446..65910573hg38UCSC Ensembl
chr9:42610762..42610889hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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