A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078541



Internal ID21987774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:898678..898678hg38UCSC Ensembl
chr5:898793..898793hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539098
Samples
Known GenesTRIP13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078541
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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