A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558728



Internal ID22427531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132883699..132884743hg38UCSC Ensembl
chr9:135759086..135760130hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349269, nssv14349272, nssv14349271, nssv14349270
SamplesNA19239, NA19240, HG00513, HG00514
Known GenesC9orf9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558728
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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