A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226067



Internal ID22369004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42538712..42539011hg38UCSC Ensembl
chr9:44215178..44215449hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38300
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346028, nssv14346027
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226067
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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