A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190155



Internal ID22341122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183886044..183886096hg38UCSC Ensembl
chr4:184807197..184807249hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14397360
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)nsv3190155
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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