A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066879



Internal ID21976112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145877317..145877317hg38UCSC Ensembl
chr5:145256880..145256880hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066879
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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