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nsv5457313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,374

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 24 studies. See in: genome view    
Submitted genomic38,679,337-38,680,710Question Mark
Overlapping variant regions from other studies: 91 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):38,647,113-38,648,486Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr638,679,33738,680,710
nsv5457313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr638,647,11338,648,486

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983669deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983669Submitted genomicNC_000006.12:g.386
79337_38680710del
GRCh38 (hg38)NC_000006.12Chr638,679,33738,680,710
nssv16983669RemappedPerfectNC_000006.11:g.386
47113_38648486del
GRCh37.p13First PassNC_000006.11Chr638,647,11338,648,486

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)
nssv16983669<0.00126404
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