A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094897



Internal ID22004130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66567894..66567894hg38UCSC Ensembl
chr16:66601797..66601797hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626582
Samples
Known GenesCKLF-CMTM1, CMTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094897
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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