A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073787



Internal ID21983020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69204071..69204071hg38UCSC Ensembl
chr5:68499898..68499898hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538118
Samples
Known GenesCENPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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