A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443496



Internal ID21101049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69379905..69564293hg38UCSC Ensembl
chr9:71994821..72179209hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38184389
hg19184389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225839
Samples
Known GenesAPBA1, FAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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