A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448366



Internal ID21105919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33376772..33408583hg38UCSC Ensembl
chr9:33376770..33408581hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3831812
hg1931812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219294
Samples
Known GenesAQP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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