A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989086



Internal ID21898429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27262190..27262286hg38UCSC Ensembl
chr2:27485058..27485154hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526902
Samples
Known GenesSLC30A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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