A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851608



Internal ID22035251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81983792..81983792hg38UCSC Ensembl
chrX:81239241..81239241hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851608
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