A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390941



Internal ID22304203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68092609..68095740hg38UCSC Ensembl
chr16:68126512..68129643hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383132
hg193132
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207058
Supporting Variants
SamplesNA19240
Known GenesNFATC3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390941
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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