A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169090



Internal ID21482337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92843643..92843643hg38UCSC Ensembl
chrX:92098642..92098642hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605239
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169090
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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