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nsv5509229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 25 studies. See in: genome view    
Submitted genomic49,867,723-49,867,786Question Mark
Overlapping variant regions from other studies: 79 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):50,261,506-50,261,569Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1249,867,72349,867,786
nsv5509229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1250,261,50650,261,569

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056417duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056417Submitted genomicNC_000012.12:g.498
67723_49867786dup
GRCh38 (hg38)NC_000012.12Chr1249,867,72349,867,786
nssv17056417RemappedPerfectNC_000012.11:g.502
61506_50261569dup
GRCh37.p13First PassNC_000012.11Chr1250,261,50650,261,569

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)
nssv17056417<0.00116404
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