A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166098



Internal ID21451567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151743041..151743041hg38UCSC Ensembl
chrX:150911513..150911513hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613748
Supporting Variants
SamplesHG01596
Known GenesCNGA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166098
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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