A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349251



Internal ID22261288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132378505..132378618hg38UCSC Ensembl
chr9:135253892..135254005hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527502
Supporting Variants
SamplesNA19238
Known GenesTTF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349251
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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