A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183066



Internal ID22337431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149079464..149079518hg38UCSC Ensembl
chr3:148797251..148797305hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454528, nssv14410305
SamplesNA19240, HG00733
Known GenesHLTF
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183066
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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