A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018281



Internal ID21927624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69796494..69797419hg38UCSC Ensembl
chr8:70708729..70709654hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580166
Samples
Known GenesSLCO5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018281
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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