A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615114



Internal ID21563419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1293845..1293845hg38UCSC Ensembl
chrX:1412738..1412738hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165665
SamplesNA24385
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615114
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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