A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583892



Internal ID21532423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172493389..172493472hg38UCSC Ensembl
chr5:171920393..171920476hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138634
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583892
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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