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nsv5469713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
Submitted genomic137,150,167-137,150,260Question Mark
Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):137,471,304-137,471,397Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5469713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6137,150,167137,150,260
nsv5469713RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6137,471,304137,471,397

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970176deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970176Submitted genomicNC_000006.12:g.137
150167_137150260de
l
GRCh38 (hg38)NC_000006.12Chr6137,150,167137,150,260
nssv16970176RemappedPerfectNC_000006.11:g.137
471304_137471397de
l
GRCh37.p13First PassNC_000006.11Chr6137,471,304137,471,397

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)
nssv16970176<0.00126404
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