A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078193



Internal ID21987426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977716..6977716hg38UCSC Ensembl
chr4:6979443..6979443hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546763
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078193
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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