A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072107



Internal ID21981340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112086829..112086829hg38UCSC Ensembl
chr6:112408032..112408032hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564035
Samples
Known GenesTUBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072107
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer