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nsv5415943

  • 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: 124 SVs from 23 studies. See in: genome view    
Submitted genomic52,230,335-52,230,386Question Mark
Overlapping variant regions from other studies: 124 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):52,522,532-52,522,583Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1552,230,33552,230,386
nsv5415943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1552,522,53252,522,583

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702748alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702748Submitted genomicNC_000015.10:g.522
30335_52230386ins2
81
GRCh38 (hg38)NC_000015.10Chr1552,230,33552,230,386
nssv17702748RemappedPerfectNC_000015.9:g.5252
2532_52522583ins28
1
GRCh37.p13First PassNC_000015.9Chr1552,522,53252,522,583

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)
nssv17702748<0.00126404
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