A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989623



Internal ID21898966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65353788..65353857hg38UCSC Ensembl
chr2:65580922..65580991hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533589
Samples
Known GenesSPRED2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989623
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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