A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259692



Internal ID22064302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109818606..109818606hg38UCSC Ensembl
chrX:109061835..109061835hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259692
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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