A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070368



Internal ID21979601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63440251..63440251hg38UCSC Ensembl
chr8:64352809..64352809hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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