A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001508



Internal ID21910851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126420722..126507923hg38UCSC Ensembl
chr8:127432967..127520168hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3887202
hg1987202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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