A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982782



Internal ID21892125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214622721..214622805hg38UCSC Ensembl
chr1:214796064..214796148hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527857
Samples
Known GenesCENPF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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