A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635651



Internal ID21583956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55897000..55897000hg38UCSC Ensembl
chr5:55192828..55192828hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155940
SamplesHG00731
Known GenesIL31RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635651
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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