A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581872



Internal ID21530377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26153223..26156004hg38UCSC Ensembl
chr2:26376092..26378873hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382782
hg192782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113948
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581872
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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