A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045143



Internal ID20612183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1697033..1781345hg38UCSC Ensembl
chr19:1697032..1781344hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3884313
hg1984313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534377
Supporting Variants
Samples
Known GenesONECUT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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