A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109722



Internal ID22018955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154257387..154277389hg38UCSC Ensembl
chrX:153485052..153501499hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3820003
hg1916448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640717
Samples
Known GenesOPN1MW, OPN1MW2, TEX28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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