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nsv5411302

  • 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: 117 SVs from 23 studies. See in: genome view    
Submitted genomic12,234,194-12,234,245Question Mark
Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):12,273,820-12,273,871Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411302Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr712,234,19412,234,245
nsv5411302RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr712,273,82012,273,871

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16993034alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16993034Submitted genomicNC_000007.14:g.122
34194_12234245ins1
17
GRCh38 (hg38)NC_000007.14Chr712,234,19412,234,245
nssv16993034RemappedPerfectNC_000007.13:g.122
73820_12273871ins1
17
GRCh37.p13First PassNC_000007.13Chr712,273,82012,273,871

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)
nssv16993034<0.00116404
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