A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166411



Internal ID21470882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18881750..18881750hg38UCSC Ensembl
chrX:18899868..18899868hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614029
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166411
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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