A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490768



Internal ID268019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93016434..93017875hg38UCSC Ensembl
chr9:95778716..95780157hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025677
Samples
Known GenesFGD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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