A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451993



Internal ID21109546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35015542..35048917hg38UCSC Ensembl
chr9:35015539..35048914hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3833376
hg1933376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226026
Samples
Known GenesC9orf131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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