A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190830



Internal ID22341635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:601175..606488hg38UCSC Ensembl
chr19:601175..606488hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385314
hg195314
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14431797, nssv14431798
SamplesHG00514
Known GenesHCN2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190830
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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