A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070626



Internal ID21979859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23940566..23940566hg38UCSC Ensembl
chr8:23798079..23798079hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070626
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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