A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452503



Internal ID22247398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158846021..158846227hg38UCSC Ensembl
chr4:159767173..159767379hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3184865
Supporting Variants
SamplesHG00733
Known GenesFNIP2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14452503
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