A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184136



Internal ID22337986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62328058..62328111hg38UCSC Ensembl
chr3:62313733..62313786hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14397433
SamplesNA19240
Known GenesC3orf14
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184136
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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