A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565258



Internal ID22433979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76180241..76180241hg38UCSC Ensembl
chr8:77092476..77092476hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343886, nssv14343885
SamplesNA19239, HG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565258
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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