A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217270



Internal ID22362980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85383162..85383251hg38UCSC Ensembl
chr9:87998077..87998166hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347856
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217270
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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