A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529213



Internal ID22398606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132028544..132028615hg38UCSC Ensembl
chr8:133040791..133040862hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9351n152
Supporting Variantsnssv14344000, nssv14344001, nssv14343999
SamplesNA19239, NA19240, HG00733
Known GenesOC90
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529213
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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