A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988027



Internal ID21897370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234901996..234902088hg38UCSC Ensembl
chr2:235810640..235810732hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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