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nsv5559915

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 34 studies. See in: genome view    
Submitted genomic84,890,383-84,890,434Question Mark
Overlapping variant regions from other studies: 148 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):85,284,162-85,284,213Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559915Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1284,890,38384,890,434
nsv5559915RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1285,284,16285,284,213

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689726line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689726Submitted genomicNC_000012.12:g.848
90383_84890434ins6
019
GRCh38 (hg38)NC_000012.12Chr1284,890,38384,890,434
nssv17689726RemappedPerfectNC_000012.11:g.852
84162_85284213ins6
019
GRCh37.p13First PassNC_000012.11Chr1285,284,16285,284,213

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)Allele Count (AC)Allele Number (AN)
nssv176897260.003216398
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