A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026201



Internal ID21935544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102379290..102379545hg38UCSC Ensembl
chr14:102845627..102845882hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602774
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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