A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439748



Internal ID22182056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66129156..66144586hg38UCSC Ensembl
chr9:42376680..42392106hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3815431
hg1915427
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200295
Supporting Variants
SamplesHG00514
Known GenesANKRD20A2, ANKRD20A3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439748
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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