A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078834



Internal ID21988067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130153332..130153332hg38UCSC Ensembl
chr8:131165578..131165578hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584066
Samples
Known GenesASAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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