A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212589



Internal ID22359786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38206011..38206331hg38UCSC Ensembl
chr8:38063529..38063849hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341228, nssv14341229
SamplesHG00731, HG00733
Known GenesBAG4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212589
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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