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nsv5506386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,189

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 166 SVs from 28 studies. See in: genome view    
Submitted genomic67,276,938-67,279,126Question Mark
Overlapping variant regions from other studies: 166 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):67,670,718-67,672,906Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1267,276,93867,279,126
nsv5506386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1267,670,71867,672,906

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688765deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688765Submitted genomicNC_000012.12:g.672
76938_67279126del
GRCh38 (hg38)NC_000012.12Chr1267,276,93867,279,126
nssv17688765RemappedPerfectNC_000012.11:g.676
70718_67672906del
GRCh37.p13First PassNC_000012.11Chr1267,670,71867,672,906

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)
nssv17688765<0.00126404
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