A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439576



Internal ID22236277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93895225..93895400hg38UCSC Ensembl
chr9:96657507..96657682hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208373
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)nssv14439576
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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