A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206804



Internal ID22355293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184318557..184318829hg38UCSC Ensembl
chr3:184036345..184036617hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310203
SamplesHG00513
Known GenesEIF4G1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206804
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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