A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529402



Internal ID22398794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85454683..85454743hg38UCSC Ensembl
chr9:88069598..88069658hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347857
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529402
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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