A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483719



Internal ID261149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81755304..81755398hg38UCSC Ensembl
chr9:84370219..84370313hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026003
Samples
Known GenesLOC101927502
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483719
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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