A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14424217



Internal ID22163529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25397944..25398152hg38UCSC Ensembl
chr4:25399566..25399774hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179787
Supporting Variants
SamplesHG00514
Known GenesANAPC4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14424217
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer