A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166504



Internal ID21474663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152182714..152182714hg38UCSC Ensembl
chrX:151351186..151351186hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623215
Supporting Variants
SamplesHG03371
Known GenesGABRA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166504
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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