A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580615



Internal ID21529107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443733..1443799hg38UCSC Ensembl
chr2:1447505..1447571hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109463
SamplesHG00731
Known GenesTPO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580615
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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