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nsv5562217

  • 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: 90 SVs from 25 studies. See in: genome view    
Submitted genomic72,106,560-72,106,611Question Mark
Overlapping variant regions from other studies: 90 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):73,866,318-73,866,369Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1072,106,56072,106,611
nsv5562217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1073,866,31873,866,369

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17035304sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17035304Submitted genomicNC_000010.11:g.721
06560_72106611ins1
276
GRCh38 (hg38)NC_000010.11Chr1072,106,56072,106,611
nssv17035304RemappedPerfectNC_000010.10:g.738
66318_73866369ins1
276
GRCh37.p13First PassNC_000010.10Chr1073,866,31873,866,369

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)
nssv170353040.002136400
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