A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224235



Internal ID22367725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74129800..74132022hg38UCSC Ensembl
chr9:76744716..76746938hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382223
hg192223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346227, nssv14346229, nssv14346228
SamplesNA19238, NA19239, NA19240
Known GenesMIR6130
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224235
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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