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nsv5536908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 20 studies. See in: genome view    
Submitted genomic166,930,620-166,930,642Question Mark
Overlapping variant regions from other studies: 180 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):167,344,108-167,344,130Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6166,930,620166,930,642
nsv5536908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,344,108167,344,130

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16991242insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16991242Submitted genomicNC_000006.12:g.166
930620_166930642in
s54
GRCh38 (hg38)NC_000006.12Chr6166,930,620166,930,642
nssv16991242RemappedPerfectNC_000006.11:g.167
344108_167344130in
s54
GRCh37.p13First PassNC_000006.11Chr6167,344,108167,344,130

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)
nssv16991242<0.00166396
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