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nsv4324370

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,373

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):53,485,583-53,514,955Question Mark
Overlapping variant regions from other studies: 122 SVs from 13 studies. See in: genome view    
Submitted genomic53,553,276-53,582,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4324370RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr753,485,58353,514,955
nsv4324370Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr753,553,27653,582,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091408inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091408RemappedPerfectNC_000007.14:g.534
85583_53514955inv
GRCh38.p12First PassNC_000007.14Chr753,485,58353,514,955
nssv16091408Submitted genomicNC_000007.13:g.535
53276_53582648inv
GRCh37.p13NC_000007.13Chr753,553,27653,582,648

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)
nssv160914080.0012921694
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