A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257154



Internal ID22061764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126543960..126543960hg38UCSC Ensembl
chr6:126865106..126865106hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257154
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