A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171818



Internal ID22331484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3308064..3311264hg38UCSC Ensembl
chr4:3309791..3312991hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14409055, nssv14409054
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171818
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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