A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226904



Internal ID22369553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137393566..137393939hg38UCSC Ensembl
chr8:138405809..138406182hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344820
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226904
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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