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nsv4578208

  • 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: 36 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):81,575,100-81,575,100Question Mark
Overlapping variant regions from other studies: 36 SVs from 7 studies. See in: genome view    
Submitted genomic81,968,879-81,968,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578208RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1281,575,10081,575,100
nsv4578208Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1281,968,87981,968,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15999687sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15999687RemappedPerfectNC_000012.12:g.815
75100_81575101ins1
240
GRCh38.p12First PassNC_000012.12Chr1281,575,10081,575,100
nssv15999687Submitted genomicNC_000012.11:g.819
68879_81968880ins1
240
GRCh37.p13NC_000012.11Chr1281,968,87981,968,879

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)
nssv159996874.6e-005121694
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