A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214236



Internal ID22360946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132377295..132377346hg38UCSC Ensembl
chr9:135252682..135252733hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349249
SamplesHG00512
Known GenesTTF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214236
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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