A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14374869



Internal ID22321357
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223655
Supporting Variants
SamplesNA19240
Known GenesTTF1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14374869
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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