A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060662



Internal ID21969895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116670205..116670205hg38UCSC Ensembl
chr8:117682444..117682444hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595286
Samples
Known GenesEIF3H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060662
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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