A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985819



Internal ID21895162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11538609..11538661hg38UCSC Ensembl
chr2:11678735..11678787hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536250
Samples
Known GenesGREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985819
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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