A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851444



Internal ID22035087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9954515..9954515hg38UCSC Ensembl
chrX:9922555..9922555hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851444
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