A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528205



Internal ID22397591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108264566..108267949hg38UCSC Ensembl
chr8:109276795..109280178hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg383384
hg193384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343018
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528205
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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