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nsv5419091

  • 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: 125 SVs from 29 studies. See in: genome view    
Submitted genomic56,454,692-56,454,743Question Mark
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):56,966,061-56,966,112Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419091Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,454,69256,454,743
nsv5419091RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,966,06156,966,112

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725790alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725790Submitted genomicNC_000019.10:g.564
54692_56454743ins2
81
GRCh38 (hg38)NC_000019.10Chr1956,454,69256,454,743
nssv17725790RemappedPerfectNC_000019.9:g.5696
6061_56966112ins28
1
GRCh37.p13First PassNC_000019.9Chr1956,966,06156,966,112

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)
nssv177257900.24915966404
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