A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989166



Internal ID21898509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41811749..41841568hg38UCSC Ensembl
chr2:42038889..42068708hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3829820
hg1929820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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