A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194457



Internal ID20761497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75446563..75450214hg38UCSC Ensembl
chr9:78061479..78065130hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383652
hg193652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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