A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166191



Internal ID21480731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20299548..20299548hg38UCSC Ensembl
chrX:20317666..20317666hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607643
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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