A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917821



Internal ID22693042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:237646..634217hg38UCSC Ensembl
chr9:237646..634217hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38396572
hg19396572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446667
Samples
Known GenesDOCK8, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917821
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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