A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065185



Internal ID21974418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54555415..54555415hg38UCSC Ensembl
chr8:55467975..55467975hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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