A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252385



Internal ID22056995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25960346..25960346hg38UCSC Ensembl
chrX:25978463..25978463hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252385
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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