A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050853



Internal ID21960087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39046285..39046285hg38UCSC Ensembl
chr2:39273426..39273426hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526072
Samples
Known GenesSOS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050853
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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