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nsv4150129

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:593

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):95,581,777-95,582,369Question Mark
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Submitted genomic96,029,653-96,030,245Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4150129RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr695,581,77795,582,369
nsv4150129Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr696,029,65396,030,245

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15910916deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15910916RemappedPerfectNC_000006.12:g.955
81777_95582369del
GRCh38.p12First PassNC_000006.12Chr695,581,77795,582,369
nssv15910916Submitted genomicNC_000006.11:g.960
29653_96030245del
GRCh37.p13NC_000006.11Chr696,029,65396,030,245

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)
nssv15910916<0.001421694
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