A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529349



Internal ID22398741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90012254..90012511hg38UCSC Ensembl
chr14:90478598..90478855hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390610, nssv14385292
SamplesHG00733, HG00514
Known GenesTDP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529349
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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