A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990238



Internal ID21899581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66350018..66353474hg38UCSC Ensembl
chr2:66577150..66580606hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383457
hg193457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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