A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067560



Internal ID21976793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10060276..10060276hg38UCSC Ensembl
chr8:9917786..9917786hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562138
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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