A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197358



Internal ID20764398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12769157..12780548hg38UCSC Ensembl
chr19:12879971..12891362hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3811392
hg1911392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525550
Supporting Variants
Samples
Known GenesHOOK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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