A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226772



Internal ID22369466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35157453..35157742hg38UCSC Ensembl
chr9:35157450..35157739hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346405, nssv14346404, nssv14346406
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226772
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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