A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034069



Internal ID21943412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102410281..102411731hg38UCSC Ensembl
chr14:102876618..102878068hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605870
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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