A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195818



Internal ID20762858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11792169..11811875hg38UCSC Ensembl
chr18:11792168..11811874hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3819707
hg1919707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528910
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195818
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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