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nsv5545714

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
Submitted genomic71,296,899-71,296,903Question Mark
Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):73,056,656-73,056,660Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5545714Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1071,296,89971,296,903
nsv5545714RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1073,056,65673,056,660

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17035232insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17035232Submitted genomicNC_000010.11:g.712
96899_71296903ins6
0
GRCh38 (hg38)NC_000010.11Chr1071,296,89971,296,903
nssv17035232RemappedPerfectNC_000010.10:g.730
56656_73056660ins6
0
GRCh37.p13First PassNC_000010.10Chr1073,056,65673,056,660

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)
nssv17035232<0.00126404
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