A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168531



Internal ID21409116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87205391..87205391hg38UCSC Ensembl
chrX:86460394..86460394hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614924
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168531
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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