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nsv5553918

  • 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: 530 SVs from 20 studies. See in: genome view    
Submitted genomic2,714,305-2,714,356Question Mark
Overlapping variant regions from other studies: 531 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):2,632,346-2,632,397Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553918Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX2,714,3052,714,356
nsv5553918RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX2,632,3462,632,397

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739043sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739043Submitted genomicNC_000023.11:g.271
4305_2714356ins124
0
GRCh38 (hg38)NC_000023.11ChrX2,714,3052,714,356
nssv17739043RemappedPerfectNC_000023.10:g.263
2346_2632397ins124
0
GRCh37.p13First PassNC_000023.10ChrX2,632,3462,632,397

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)
nssv17739043<0.00146404
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