A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635521



Internal ID21583826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55959212..55959212hg38UCSC Ensembl
chr5:55255040..55255040hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149483
SamplesHG00513
Known GenesIL6ST
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635521
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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