A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252383



Internal ID22056993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25286787..25286787hg38UCSC Ensembl
chrX:25304904..25304904hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252383
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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