A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668284



Internal ID21616589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35609324..35616275hg38UCSC Ensembl
chrX:35627441..35634392hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386952
hg196952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166826
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668284
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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