A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544553



Internal ID21868908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:628499..628499hg38UCSC Ensembl
chr5:628614..628614hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063974
Supporting Variants
Samples
Known GenesCEP72
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544553
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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