A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397356



Internal ID22304146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183794649..183795635hg38UCSC Ensembl
chr4:184715802..184716788hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179253
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)nssv14397356
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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