A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252323



Internal ID22056933
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 StatusM
Merged Variants
Supporting Variantsnssv17851469
Samples
Known GenesPIR, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252323
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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