A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174076



Internal ID20741116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115944015..115944420hg38UCSC Ensembl
chr9:118706294..118706699hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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