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nsv5556693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Submitted genomic31,535,637-31,535,672Question Mark
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):31,503,414-31,503,449Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5556693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,535,63731,535,672
nsv5556693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,503,41431,503,449

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16980418sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16980418Submitted genomicNC_000006.12:g.315
35637_31535672ins1
240
GRCh38 (hg38)NC_000006.12Chr631,535,63731,535,672
nssv16980418RemappedPerfectNC_000006.11:g.315
03414_31503449ins1
240
GRCh37.p13First PassNC_000006.11Chr631,503,41431,503,449

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)
nssv16980418<0.00126404
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