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nsv5302794

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:217

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 38 studies. See in: genome view    
Submitted genomic43,067,766-43,068,317Question Mark
Overlapping variant regions from other studies: 129 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):43,035,504-43,036,055Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5302794Submitted genomicGRCh38.p13Primary AssemblyNC_000006.12Chr643,067,829 (-63)43,068,045 (+272)
nsv5302794RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr643,035,567 (-63)43,035,783 (+272)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16858465deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16858465Submitted genomicNC_000006.12:g.(43
067766_?)_(?_43068
317)del
GRCh38.p13NC_000006.12Chr643,067,829 (-63)43,068,045 (+272)
nssv16858465RemappedPerfectNC_000006.11:g.(43
035504_?)_(?_43036
055)del
GRCh37.p13First PassNC_000006.11Chr643,035,567 (-63)43,035,783 (+272)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv168584650.122
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