A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042813



Internal ID21952125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986772..32986772hg38UCSC Ensembl
chr1:33452373..33452373hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042813
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