A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229232



Internal ID22371141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84797744..84797810hg38UCSC Ensembl
chr9:87412659..87412725hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347834
SamplesHG00732
Known GenesNTRK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229232
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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