A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404206



Internal ID22294535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109524406..109524519hg38UCSC Ensembl
chr9:112286686..112286799hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207677
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)nssv14404206
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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