A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199303



Internal ID22348907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46753545..46809731hg38UCSC Ensembl
chr3:46795035..46851221hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3856187
hg1956187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5960n152
Supporting Variantsnssv14306928, nssv14306927, nssv14306929
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199303
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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