A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229754



Internal ID22371497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113625011..113625160hg38UCSC Ensembl
chr13:114279326..114279475hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2500n152
Supporting Variantsnssv14372283
SamplesNA19240
Known GenesTFDP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229754
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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