A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229803



Internal ID22371532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126596864..126597254hg38UCSC Ensembl
chr9:129359143..129359533hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347758, nssv14347759, nssv14347757, nssv14347756
SamplesHG00512, NA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229803
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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