A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529432



Internal ID22398824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18942027..18942109hg38UCSC Ensembl
chr9:18942025..18942107hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345487, nssv14345486
SamplesNA19238, NA19240
Known GenesFAM154A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529432
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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