A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922782



Internal ID22698007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107225108..107225240hg38UCSC Ensembl
chr9:109987389..109987521hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922782
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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