A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206484



Internal ID22355018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10347193..10347248hg38UCSC Ensembl
chr5:10347305..10347360hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320189
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206484
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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