A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025288



Internal ID84586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78075333..78075446hg38UCSC Ensembl
chr9:80690249..80690362hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025288
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00906


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