A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486946



Internal ID264296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23855709..23855815hg38UCSC Ensembl
chr9:23855707..23855813hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486946
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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