A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527995



Internal ID22397381
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348455, nssv14348456, nssv14348454, nssv14348453
SamplesHG00512, HG00731, NA19240, HG00513
Known GenesPKN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527995
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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