A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754141



Internal ID20530001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59152239..59152239hg38UCSC Ensembl
chr18:56819471..56819471hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280506
Samples
Known GenesSEC11C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754141
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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