A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009968



Internal ID21919311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69207541..69207600hg38UCSC Ensembl
chr5:68503368..68503427hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550721
Samples
Known GenesCENPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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