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nsv5537855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 18 studies. See in: genome view    
Submitted genomic99,421,496-99,421,503Question Mark
Overlapping variant regions from other studies: 107 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):99,869,372-99,869,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5537855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr699,421,49699,421,503
nsv5537855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr699,869,37299,869,379

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16986532insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16986532Submitted genomicNC_000006.12:g.994
21496_99421503ins9
9
GRCh38 (hg38)NC_000006.12Chr699,421,49699,421,503
nssv16986532RemappedPerfectNC_000006.11:g.998
69372_99869379ins9
9
GRCh37.p13First PassNC_000006.11Chr699,869,37299,869,379

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)
nssv16986532<0.00146404
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