A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558074



Internal ID22426877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109523565..109524282hg38UCSC Ensembl
chr9:112285845..112286562hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348324, nssv14348322, nssv14348323, nssv14348326, nssv14348320, nssv14348321, nssv14348325, nssv14348319, nssv14348318
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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