A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191219



Internal ID20758259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25349101..25354000hg38UCSC Ensembl
chr18:22929065..22933964hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515770
Supporting Variants
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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