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nsv5536426

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 27 studies. See in: genome view    
Submitted genomic40,997,430-40,997,430Question Mark
Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):39,153,682-39,153,682Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536426Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,997,43040,997,430
nsv5536426RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,153,68239,153,682

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713139insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713139Submitted genomicNC_000017.11:g.409
97430_40997431ins4
76
GRCh38 (hg38)NC_000017.11Chr1740,997,43040,997,430
nssv17713139RemappedPerfectNC_000017.10:g.391
53682_39153683ins4
76
GRCh37.p13First PassNC_000017.10Chr1739,153,68239,153,682

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)
nssv17713139<0.00116404
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