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nsv5409018

  • 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: 133 SVs from 28 studies. See in: genome view    
Submitted genomic80,491,874-80,491,925Question Mark
Overlapping variant regions from other studies: 133 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):82,251,630-82,251,681Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409018Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1080,491,87480,491,925
nsv5409018RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1082,251,63082,251,681

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037135alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037135Submitted genomicNC_000010.11:g.804
91874_80491925ins2
53
GRCh38 (hg38)NC_000010.11Chr1080,491,87480,491,925
nssv17037135RemappedPerfectNC_000010.10:g.822
51630_82251681ins2
53
GRCh37.p13First PassNC_000010.10Chr1082,251,63082,251,681

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)
nssv17037135<0.00116404
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