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nsv4318291

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:323,630

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 332 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):77,435,586-77,759,215Question Mark
Overlapping variant regions from other studies: 332 SVs from 19 studies. See in: genome view    
Submitted genomic78,347,822-78,671,450Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4318291RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr877,435,58677,759,215
nsv4318291Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr878,347,82278,671,450

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090424inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090424RemappedPerfectNC_000008.11:g.774
35586_77759215inv
GRCh38.p12First PassNC_000008.11Chr877,435,58677,759,215
nssv16090424Submitted genomicNC_000008.10:g.783
47822_78671450inv
GRCh37.p13NC_000008.10Chr878,347,82278,671,450

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)
nssv160904244.6e-005121694
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