A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281621



Internal ID20490839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26829084..26829502hg38UCSC Ensembl
chr18:24409048..24409466hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281621
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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