A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046538



Internal ID20613578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45893921..45895286hg38UCSC Ensembl
chr19:46397179..46398544hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523152
Supporting Variants
Samples
Known GenesMYPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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