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nsv5554434

  • 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: 107 SVs from 17 studies. See in: genome view    
Submitted genomic49,852,818-49,852,869Question Mark
Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):48,469,355-48,469,406Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2049,852,81849,852,869
nsv5554434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2048,469,35548,469,406

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732850sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732850Submitted genomicNC_000020.11:g.498
52818_49852869ins1
226
GRCh38 (hg38)NC_000020.11Chr2049,852,81849,852,869
nssv17732850RemappedPerfectNC_000020.10:g.484
69355_48469406ins1
226
GRCh37.p13First PassNC_000020.10Chr2048,469,35548,469,406

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)
nssv177328500.007476390
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