A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217027



Internal ID22362824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38055739..38056281hg38UCSC Ensembl
chr8:37913257..37913799hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341216
SamplesHG00512
Known GenesEIF4EBP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217027
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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