A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613159



Internal ID21561464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3549355..3549355hg38UCSC Ensembl
chrX:3467396..3467396hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166821
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613159
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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