A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989792



Internal ID21899135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65641144..65642494hg38UCSC Ensembl
chr2:65868278..65869628hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989792
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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