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nsv4574905

  • 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: 63 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):46,797,220-46,797,220Question Mark
Overlapping variant regions from other studies: 63 SVs from 5 studies. See in: genome view    
Submitted genomic47,371,355-47,371,355Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4574905RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1346,797,22046,797,220
nsv4574905Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1347,371,35547,371,355

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16005437sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16005437RemappedPerfectNC_000013.11:g.467
97220_46797221ins3
96
GRCh38.p12First PassNC_000013.11Chr1346,797,22046,797,220
nssv16005437Submitted genomicNC_000013.10:g.473
71355_47371356ins3
96
GRCh37.p13NC_000013.10Chr1347,371,35547,371,355

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)
nssv160054374.6e-005121694
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