A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224794



Internal ID22368118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42067132..42071863hg38UCSC Ensembl
chr8:41924650..41929381hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg384732
hg194732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340993
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224794
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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