A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260467



Internal ID22065077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68660594..68660594hg38UCSC Ensembl
chr5:67956421..67956421hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260467
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