A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067386



Internal ID21976619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137754952..137754952hg38UCSC Ensembl
chr8:138767195..138767195hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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