A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051056



Internal ID21960290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111755128..111755128hg38UCSC Ensembl
chr1:112297750..112297750hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529829
Samples
Known GenesFAM212B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051056
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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