A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849193



Internal ID22032836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41303049..41303049hg38UCSC Ensembl
chrX:41162302..41162302hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849193
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