A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542360



Internal ID316787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100019634..100019654hg38UCSC Ensembl
chr9:102781916..102781936hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025541
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542360
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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