A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851872



Internal ID22035515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103545981..103545981hg38UCSC Ensembl
chrX:102800909..102800909hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851872
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