A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166889



Internal ID21510223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22224947..22224947hg38UCSC Ensembl
chrX:22243064..22243064hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610099
Supporting Variants
SamplesNA24385
Known GenesPHEX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166889
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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