A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068949



Internal ID21978182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:474654..474654hg38UCSC Ensembl
chr5:474769..474769hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550844
Samples
Known GenesSLC9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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