A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220367



Internal ID20787407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64059501..64107300hg38UCSC Ensembl
chrUn_gl000211:91054..138853hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3847800
hg1947800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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