A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224923



Internal ID22368212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86176020..86181514hg38UCSC Ensembl
chr8:87188249..87193743hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385495
hg195495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341949, nssv14341950
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224923
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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