A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199627



Internal ID20766667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55346595..55385047hg38UCSC Ensembl
chr19:55857963..55896415hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3838453
hg1938453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515862
Supporting Variants
Samples
Known GenesCOX6B2, FAM71E2, IL11, SUV420H2, TMEM190, TMEM238
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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