A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487845



Internal ID265171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13422364..13422459hg38UCSC Ensembl
chr9:13422363..13422458hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020522
Samples
Known GenesFLJ41200
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487845
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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