A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016891



Internal ID21926234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141252845..141252916hg38UCSC Ensembl
chr8:142262944..142263015hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590234
Samples
Known GenesSLC45A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016891
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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