A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182795



Internal ID20749835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11608401..11610600hg38UCSC Ensembl
chr18:11608400..11610599hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526426
Supporting Variants
Samples
Known GenesSLC35G4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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