A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074164



Internal ID21983397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:487339..487339hg38UCSC Ensembl
chr5:487454..487454hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553029
Samples
Known GenesSLC9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074164
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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