A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214435



Internal ID22361095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119250031..119250110hg38UCSC Ensembl
chr9:122012309..122012388hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349186, nssv14349187
SamplesHG00731, HG00733
Known GenesBRINP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214435
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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