A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217892



Internal ID22363415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97138861..97141977hg38UCSC Ensembl
chr9:99901143..99904259hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383117
hg193117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349653, nssv14349654, nssv14349655
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217892
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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