A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065362



Internal ID21974595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185999473..185999473hg38UCSC Ensembl
chr4:186920627..186920627hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065362
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