A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987736



Internal ID21897079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227426486..227434870hg38UCSC Ensembl
chr2:228291202..228299586hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg388385
hg198385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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