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nsv5492117

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:337

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 25 studies. See in: genome view    
Submitted genomic68,400,442-68,400,778Question Mark
Overlapping variant regions from other studies: 88 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):70,160,199-70,160,535Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492117Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1068,400,44268,400,778
nsv5492117RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1070,160,19970,160,535

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037425deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037425Submitted genomicNC_000010.11:g.684
00442_68400778del
GRCh38 (hg38)NC_000010.11Chr1068,400,44268,400,778
nssv17037425RemappedPerfectNC_000010.10:g.701
60199_70160535del
GRCh37.p13First PassNC_000010.10Chr1070,160,19970,160,535

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)
nssv17037425<0.00126404
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