A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166263



Internal ID21448471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149108651..149108651hg38UCSC Ensembl
chrX:148190181..148190181hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613055
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166263
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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