A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194057



Internal ID20761097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64075501..64097700hg38UCSC Ensembl
chrUn_gl000211:107054..129253hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822200
hg1922200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0026


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