A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202306



Internal ID22351489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5796255..5796548hg38UCSC Ensembl
chr5:5796368..5796661hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14319397, nssv14319396
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202306
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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