A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397867



Internal ID22303265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25988555..25989023hg38UCSC Ensembl
chr4:25990177..25990645hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182652
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)nssv14397867
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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