A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206885



Internal ID22355362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2819290..2821133hg38UCSC Ensembl
chr5:2819404..2821247hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320785, nssv14320784
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206885
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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