A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407311



Internal ID22285277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876704..880871hg38UCSC Ensembl
chr19:876704..880871hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384168
hg194168
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206337
Supporting Variants
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)nssv14407311
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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