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nsv5500616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
Submitted genomic48,672,380-48,672,490Question Mark
Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):49,066,163-49,066,273Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1248,672,38048,672,490
nsv5500616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1249,066,16349,066,273

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058183deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058183Submitted genomicNC_000012.12:g.486
72380_48672490del
GRCh38 (hg38)NC_000012.12Chr1248,672,38048,672,490
nssv17058183RemappedPerfectNC_000012.11:g.490
66163_49066273del
GRCh37.p13First PassNC_000012.11Chr1249,066,16349,066,273

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)
nssv17058183<0.00116404
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