A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926989



Internal ID22702217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32420100..32420168hg38UCSC Ensembl
chr9:32420098..32420166hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449600
Samples
Known GenesACO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926989
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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