A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583895



Internal ID21532426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132680633..132680702hg38UCSC Ensembl
chr5:132016325..132016394hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121362
SamplesHG00513
Known GenesIL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583895
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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