A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259689



Internal ID22064299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109421007..109421007hg38UCSC Ensembl
chrX:108664236..108664236hg19UCSC Ensembl
CytobandXq22.3
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 Variantsnssv17851895
Samples
Known GenesGUCY2F
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259689
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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