A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985078



Internal ID21894421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101303741..101303826hg38UCSC Ensembl
chr2:101920203..101920288hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531741
Samples
Known GenesRNF149
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985078
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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