A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210336



Internal ID22358272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34907820..34907877hg38UCSC Ensembl
chr5:34907925..34907982hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14319158, nssv14319160, nssv14319159
SamplesNA19238, NA19239, NA19240
Known GenesRAD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210336
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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