A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450991



Internal ID21108544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128060592..128064177hg38UCSC Ensembl
chr9:130822871..130826456hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383586
hg193586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236837
Samples
Known GenesNAIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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