A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492699



Internal ID269904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103916002..103916916hg38UCSC Ensembl
chr9:106678283..106679197hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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