A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072223



Internal ID21981456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93708036..93708036hg38UCSC Ensembl
chr6:94417754..94417754hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569208
Samples
Known GenesTSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072223
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