A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079166



Internal ID21988399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123733256..123733256hg38UCSC Ensembl
chr8:124745496..124745496hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595076
Samples
Known GenesANXA13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079166
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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