A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450232



Internal ID21107785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113484164..113489969hg38UCSC Ensembl
chr9:116246444..116252249hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385806
hg195806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174402
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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