A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211291



Internal ID22358896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72024622..72024760hg38UCSC Ensembl
chr9:74639538..74639676hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346175, nssv14346173, nssv14346174
SamplesHG00731, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211291
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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