A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986433



Internal ID21895776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016319..15057664hg38UCSC Ensembl
chr2:15156443..15197788hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3841346
hg1941346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986433
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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