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nsv4578226

  • 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: 59 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):85,593,581-85,593,581Question Mark
Overlapping variant regions from other studies: 59 SVs from 8 studies. See in: genome view    
Submitted genomic86,136,812-86,136,812Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578226RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1585,593,58185,593,581
nsv4578226Submitted genomicGRCh37.p13Primary AssemblyNC_000015.9Chr1586,136,81286,136,812

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16012761sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16012761RemappedPerfectNC_000015.10:g.855
93581_85593582ins3
61
GRCh38.p12First PassNC_000015.10Chr1585,593,58185,593,581
nssv16012761Submitted genomicNC_000015.9:g.8613
6812_86136813ins36
1
GRCh37.p13NC_000015.9Chr1586,136,81286,136,812

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)
nssv16012761<0.001421686
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