A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851469



Internal ID22035112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15401372..15401372hg38UCSC Ensembl
chrX:15419494..15419494hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252323
Supporting Variants
Samples
Known GenesPIR, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851469
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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