A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581160



Internal ID21529656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237565800..237565851hg38UCSC Ensembl
chr2:238474443..238474494hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111952
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581160
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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