A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386339



Internal ID22301188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:998542..998640hg38UCSC Ensembl
chr9:998542..998640hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197871
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)nssv14386339
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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