A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669020



Internal ID21617325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154634731..154646422hg38UCSC Ensembl
chrX:153862997..153874696hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811692
hg1911700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166297
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669020
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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