A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077061



Internal ID21986294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72865993..72865993hg38UCSC Ensembl
chr5:72161820..72161820hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546482
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077061
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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