A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165590



Internal ID21429793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118784108..118784108hg38UCSC Ensembl
chrX:117918071..117918071hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624055
Supporting Variants
SamplesHG00731
Known GenesIL13RA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165590
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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