A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198893



Internal ID20765933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45649971..45661746hg38UCSC Ensembl
chr19:46153229..46165004hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3811776
hg1911776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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