A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271679



Internal ID20480897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13379972..13379972hg38UCSC Ensembl
chr18:13379971..13379971hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752267
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271679
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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