A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668268



Internal ID21616573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154180522..154255464hg38UCSC Ensembl
chrX:153446010..153520406hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3874943
hg1974397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166130
SamplesHG00732
Known GenesOPN1MW, OPN1MW2, TEX28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668268
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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