A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220592



Internal ID20787632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108527501..108532500hg38UCSC Ensembl
chr9:111289781..111294780hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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