A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166109



Internal ID21480743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153405995..153405995hg38UCSC Ensembl
chrX:152671453..152671453hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610805
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166109
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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