A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527183



Internal ID22396568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89483670..89483734hg38UCSC Ensembl
chr9:92098585..92098649hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348803, nssv14348806, nssv14348807, nssv14348804, nssv14348805
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527183
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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