A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214803



Internal ID22361341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30895298..30895701hg38UCSC Ensembl
chr8:30752814..30753217hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340425, nssv14340426
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214803
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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