A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018027



Internal ID21927370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144413118..144413180hg38UCSC Ensembl
chr8:145638502..145638564hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592124
Samples
Known GenesSLC39A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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