A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062480



Internal ID21971713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73880587..73880587hg38UCSC Ensembl
chr8:74792822..74792822hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062480
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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