A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166309



Internal ID21500282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155282327..155282327hg38UCSC Ensembl
chrX:154511616..154511616hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615334
Supporting Variants
SamplesNA19239
Known GenesCLIC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166309
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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