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nsv5525583

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:316

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 30 studies. See in: genome view    
Submitted genomic68,552,665-68,552,980Question Mark
Overlapping variant regions from other studies: 127 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):66,548,806-66,549,121Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525583Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1768,552,66568,552,980
nsv5525583RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1766,548,80666,549,121

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714227deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714227Submitted genomicNC_000017.11:g.685
52665_68552980del
GRCh38 (hg38)NC_000017.11Chr1768,552,66568,552,980
nssv17714227RemappedPerfectNC_000017.10:g.665
48806_66549121del
GRCh37.p13First PassNC_000017.10Chr1766,548,80666,549,121

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)
nssv177142270.1459276404
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