A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077654



Internal ID21986887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77000370..77000370hg38UCSC Ensembl
chr8:77912606..77912606hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594962
Samples
Known GenesPEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077654
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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