A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397360



Internal ID22300469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183886044..183886096hg38UCSC Ensembl
chr4:184807197..184807249hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190155
Supporting Variants
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)nssv14397360
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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