A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193563



Internal ID20760603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31893196..32005935hg38UCSC Ensembl
chr18:29473159..29585898hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38112740
hg19112740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523180
Supporting Variants
Samples
Known GenesTRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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