A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234866



Internal ID20801906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65392001..65397500hg38UCSC Ensembl
chr9:45734525..45740024hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437202
Supporting Variants
Samples
Known GenesFAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.40339


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