A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870284



Internal ID22645220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31937668..31940422hg38UCSC Ensembl
chr18:29517631..29520385hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479607
Samples
Known GenesTRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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