A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076418



Internal ID21985651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87616881..87616881hg38UCSC Ensembl
chr8:88629109..88629109hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076418
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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