A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216739



Internal ID20783779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161054835..161169282hg38UCSC Ensembl
chr6:161475867..161590314hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38114448
hg19114448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612989
Supporting Variants
Samples
Known GenesAGPAT4, AGPAT4-IT1, MAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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