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nsv4578219

  • 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: 46 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):57,100,917-57,100,917Question Mark
Overlapping variant regions from other studies: 46 SVs from 6 studies. See in: genome view    
Submitted genomic57,134,829-57,134,829Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578219RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1657,100,91757,100,917
nsv4578219Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1657,134,82957,134,829

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16014109sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16014109RemappedPerfectNC_000016.10:g.571
00917_57100918ins8
56
GRCh38.p12First PassNC_000016.10Chr1657,100,91757,100,917
nssv16014109Submitted genomicNC_000016.9:g.5713
4829_57134830ins85
6
GRCh37.p13NC_000016.9Chr1657,134,82957,134,829

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)
nssv160141094.6e-005121694
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