A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348455



Internal ID22190824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128709777..128710053hg38UCSC Ensembl
chr9:131472056..131472332hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527995
Supporting Variants
SamplesHG00731
Known GenesPKN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348455
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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