A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986076



Internal ID21895419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121225771..121225887hg38UCSC Ensembl
chr2:121983347..121983463hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529312
Samples
Known GenesTFCP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986076
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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