A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180434



Internal ID22336066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84900416..84915591hg38UCSC Ensembl
chr3:84949567..84964742hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3815176
hg1915176
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6055n152
Supporting Variantsnssv14423108
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180434
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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