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nsv4573574

  • 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: 27 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):16,183,560-16,183,560Question Mark
Overlapping variant regions from other studies: 27 SVs from 7 studies. See in: genome view    
Submitted genomic16,294,371-16,294,371Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573574RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1916,183,56016,183,560
nsv4573574Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1916,294,37116,294,371

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16022621sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16022621RemappedPerfectNC_000019.10:g.161
83560_16183561ins1
235
GRCh38.p12First PassNC_000019.10Chr1916,183,56016,183,560
nssv16022621Submitted genomicNC_000019.9:g.1629
4371_16294372ins12
35
GRCh37.p13NC_000019.9Chr1916,294,37116,294,371

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)
nssv16022621<0.001721682
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