A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671566



Internal ID21619871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78260513..78268590hg38UCSC Ensembl
chrX:77516010..77524087hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg388078
hg198078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168188
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671566
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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