A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259499



Internal ID22064109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63813885..63813885hg38UCSC Ensembl
chrX:63033765..63033765hg19UCSC Ensembl
CytobandXq11.2
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 Variantsnssv17850893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259499
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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