A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066919



Internal ID21976152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183183395..183183395hg38UCSC Ensembl
chr4:184104548..184104548hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547337
Samples
Known GenesWWC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066919
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