A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195190



Internal ID22345407
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 Variantsnssv14409336
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195190
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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