A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220856



Internal ID20787896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33329002..33387398hg38UCSC Ensembl
chr9:33329000..33387396hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3858397
hg1958397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442909
Supporting Variants
Samples
Known GenesAQP7, NFX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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