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nsv5553035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
Submitted genomic130,837,414-130,837,448Question Mark
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):131,158,554-131,158,588Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6130,837,414130,837,448
nsv5553035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6131,158,554131,158,588

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16969740insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16969740Submitted genomicNC_000006.12:g.130
837414_130837448in
s256
GRCh38 (hg38)NC_000006.12Chr6130,837,414130,837,448
nssv16969740RemappedPerfectNC_000006.11:g.131
158554_131158588in
s256
GRCh37.p13First PassNC_000006.11Chr6131,158,554131,158,588

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)
nssv16969740<0.00116404
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