A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166343



Internal ID21511997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:156009241..156009241hg38UCSC Ensembl
chrX:155238906..155238906hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622070
Supporting Variants
SamplesNA24385
Known GenesIL9R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166343
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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