A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534833



Internal ID310585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90465429..90465475hg38UCSC Ensembl
chr9:93227711..93227757hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024005
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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