A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190063



Internal ID22341080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57990146..57990222hg38UCSC Ensembl
chr4:58856312..58856388hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460237
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190063
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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