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nsv4573517

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 10 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):25,482,088-25,482,088Question Mark
Overlapping variant regions from other studies: 10 SVs from 3 studies. See in: genome view    
Submitted genomic25,482,316-25,482,316Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573517RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr625,482,08825,482,088
nsv4573517Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr625,482,31625,482,316

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16067067line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16067067RemappedPerfectNC_000006.12:g.254
82088_25482089ins6
018
GRCh38.p12First PassNC_000006.12Chr625,482,08825,482,088
nssv16067067Submitted genomicNC_000006.11:g.254
82316_25482317ins6
018
GRCh37.p13NC_000006.11Chr625,482,31625,482,316

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)
nssv160670674.6e-005121694
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