A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580413



Internal ID21528903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65448903..65449261hg38UCSC Ensembl
chr2:65676037..65676395hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113555
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580413
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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