A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213724



Internal ID22360580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66337937..66338003hg38UCSC Ensembl
chr9:42183748..42183802hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9576n152
Supporting Variantsnssv14346794, nssv14346795, nssv14346793, nssv14346791, nssv14346792, nssv14346796, nssv14346797
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213724
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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