A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062314



Internal ID21971547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60668209..60668209hg38UCSC Ensembl
chr5:59964036..59964036hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541742
Samples
Known GenesDEPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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