A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381091



Internal ID22438961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31940584..31940910hg38UCSC Ensembl
chr18:29520547..29520873hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936383
Supporting Variants
Samples
Known GenesTRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381091
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.066


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