A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064031



Internal ID21973264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3074615..3074615hg38UCSC Ensembl
chr4:3076342..3076342hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064031
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