A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562138



Internal ID21886493
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 StatusS
Merged Variantsnsv6067560
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562138
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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