A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806891



Internal ID21252229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28458370..28458858hg38UCSC Ensembl
chr2:28681237..28681725hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806891
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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