A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232569



Internal ID20799609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120630801..120640700hg38UCSC Ensembl
chr9:123393079..123402978hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454417
Supporting Variants
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00056


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