A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186563



Internal ID22339269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37460968..37462157hg38UCSC Ensembl
chr4:37462590..37463779hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14409164
SamplesNA19240
Known GenesC4orf19
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186563
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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