A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091608



Internal ID22000841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25278668..25278668hg38UCSC Ensembl
chr13:25852806..25852806hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610280
Samples
Known GenesMTMR6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091608
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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