A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443227



Internal ID21100780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132883703..132884881hg38UCSC Ensembl
chr9:135759090..135760268hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229141
Samples
Known GenesC9orf9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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