A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349187



Internal ID22234145
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214435
Supporting Variants
SamplesHG00733
Known GenesBRINP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349187
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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