A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449168



Internal ID21106721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33961320..34119929hg38UCSC Ensembl
chr9:33961318..34119927hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38158610
hg19158610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236571
Samples
Known GenesDCAF12, UBAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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