A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850907



Internal ID22034550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69329674..69329674hg38UCSC Ensembl
chrX:68549517..68549517hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850907
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