A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206337



Internal ID22354894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876704..880871hg38UCSC Ensembl
chr19:876704..880871hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384168
hg194168
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4050n152
Supporting Variantsnssv14407310, nssv14407311
SamplesNA19240
Known GenesMED16
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206337
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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