A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210019



Internal ID22358006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175266583..175266664hg38UCSC Ensembl
chr5:174693586..174693667hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7626n152
Supporting Variantsnssv14324594, nssv14324595
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210019
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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