A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064578



Internal ID21973811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17273671..17273671hg38UCSC Ensembl
chr5:17273780..17273780hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557433
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064578
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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