A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198095



Internal ID20765135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37981495..37999479hg38UCSC Ensembl
chr19:38472135..38490119hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3817985
hg1917985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517965
Supporting Variants
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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