A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463241



Internal ID22215760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87925015..87938528hg38UCSC Ensembl
chr4:88846167..88859680hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3813514
hg1913514
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180874
Supporting Variants
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)nssv14463241
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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