A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213774



Internal ID22360612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107565463..107566009hg38UCSC Ensembl
chr9:110327744..110328290hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348273, nssv14348274
SamplesHG00731, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213774
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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