A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610099



Internal ID21558404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22224947..22224947hg38UCSC Ensembl
chrX:22243064..22243064hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166889, nssv17166888
SamplesHG00731, NA24385
Known GenesPHEX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610099
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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