A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062373



Internal ID21971606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123449949..123449949hg38UCSC Ensembl
chr8:124462189..124462189hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062373
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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