A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565131



Internal ID22433853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102867903..102867903hg38UCSC Ensembl
chr8:103880131..103880131hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342210, nssv14342208, nssv14342211, nssv14342209
SamplesHG00512, HG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565131
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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