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nsv5426104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 26 studies. See in: genome view    
Submitted genomic46,812,732-46,812,783Question Mark
Overlapping variant regions from other studies: 121 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):46,846,644-46,846,695Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5426104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1646,812,73246,812,783
nsv5426104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1646,846,64446,846,695

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709339alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709339Submitted genomicNC_000016.10:g.468
12732_46812783ins2
81
GRCh38 (hg38)NC_000016.10Chr1646,812,73246,812,783
nssv17709339RemappedPerfectNC_000016.9:g.4684
6644_46846695ins28
1
GRCh37.p13First PassNC_000016.9Chr1646,846,64446,846,695

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)
nssv17709339<0.00116404
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