A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065092



Internal ID21974325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8788881..8788881hg38UCSC Ensembl
chr4:8790607..8790607hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065092
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