A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14410449



Internal ID22289086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165081465..165083902hg38UCSC Ensembl
chr4:166002617..166005054hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188203
Supporting Variants
SamplesNA19240
Known GenesTMEM192
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14410449
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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