A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236571



Internal ID20803611
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 StatusS
Merged Variantsnsv6449168
Supporting Variants
Samples
Known GenesDCAF12, UBAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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