A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166920



Internal ID21449675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24362872..24362872hg38UCSC Ensembl
chrX:24380989..24380989hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613007
Supporting Variants
SamplesHG01114
Known GenesSUPT20HL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166920
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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