A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076998



Internal ID21986231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194327748..194327748hg38UCSC Ensembl
chr3:194048477..194048477hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076998
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