A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060116



Internal ID21969349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22956135..22956135hg38UCSC Ensembl
chr1:23282628..23282628hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060116
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