A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246124



Internal ID22050734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72043294..72043294hg38UCSC Ensembl
chr8:72955529..72955529hg19UCSC Ensembl
Cytoband8q13.3
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 Variantsnssv17840602
Samples
Known GenesLOC100132891, TRPA1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246124
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