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nsv5550263

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 23 studies. See in: genome view    
Submitted genomic53,898,930-53,898,933Question Mark
Overlapping variant regions from other studies: 104 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):54,402,184-54,402,187Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5550263Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,898,93053,898,933
nsv5550263RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,402,18454,402,187

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724320insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724320Submitted genomicNC_000019.10:g.538
98930_53898933ins8
9
GRCh38 (hg38)NC_000019.10Chr1953,898,93053,898,933
nssv17724320RemappedPerfectNC_000019.9:g.5440
2184_54402187ins89
GRCh37.p13First PassNC_000019.9Chr1954,402,18454,402,187

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)
nssv177243200.0613836262
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