A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565197



Internal ID22433918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121936815..121936815hg38UCSC Ensembl
chr8:122949054..122949054hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344236, nssv14344237
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565197
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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