A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492983



Internal ID270176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547258..78553856hg38UCSC Ensembl
chr9:81162174..81168772hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg386599
hg196599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv546n206
Supporting Variantsnssv17024441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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