A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060148



Internal ID21969381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108023450..108023450hg38UCSC Ensembl
chr1:108566072..108566072hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060148
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