A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439319



Internal ID22232078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137840166..137843634hg38UCSC Ensembl
chr9:140734618..140738086hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383469
hg193469
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194766
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439319
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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