A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561915



Internal ID21886270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161265502..161265502hg38UCSC Ensembl
chr6:161686534..161686534hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060589
Supporting Variants
Samples
Known GenesAGPAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561915
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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