A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946810



Internal ID22722307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78818238..78818310hg38UCSC Ensembl
chr18:76578238..76578310hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946810
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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