A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261225



Internal ID22065835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27112837..27112837hg38UCSC Ensembl
chr7:27152456..27152456hg19UCSC Ensembl
Cytoband7p15.2
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 Variantsnssv17859969
Samples
Known GenesHOXA3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261225
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