A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347834



Internal ID22208458
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229232
Supporting Variants
SamplesHG00732
Known GenesNTRK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347834
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer