A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256716



Internal ID22061326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19159911..19159911hg38UCSC Ensembl
chr1:19486405..19486405hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857315
Samples
Known GenesUBR4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256716
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer