A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259496



Internal ID22064106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62463346..62463346hg38UCSC Ensembl
chrX:61682816..61682816hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259496
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