A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752267



Internal ID20528127
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 StatusM
Merged Variants
Supporting Variantsnssv16271679
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752267
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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