A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616814



Internal ID21565119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22346954..22346954hg38UCSC Ensembl
chrX:22365071..22365071hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166656
SamplesNA19238
Known GenesLOC100873065
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616814
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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