A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106066



Internal ID22015299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154148235..154219586hg38UCSC Ensembl
chrX:153413708..153485055hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3871352
hg1971348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637585
Samples
Known GenesOPN1LW, OPN1MW, OPN1MW2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer