A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252390



Internal ID22057000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26473044..26473044hg38UCSC Ensembl
chrX:26491161..26491161hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252390
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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