A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068826



Internal ID21978059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122950885..122950885hg38UCSC Ensembl
chr8:123963125..123963125hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584100
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068826
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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