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nsv5528892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 31 studies. See in: genome view    
Submitted genomic84,595,941-84,596,059Question Mark
Overlapping variant regions from other studies: 183 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):84,629,547-84,629,665Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,595,94184,596,059
nsv5528892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,629,54784,629,665

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17708336duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17708336Submitted genomicNC_000016.10:g.845
95941_84596059dup
GRCh38 (hg38)NC_000016.10Chr1684,595,94184,596,059
nssv17708336RemappedPerfectNC_000016.9:g.8462
9547_84629665dup
GRCh37.p13First PassNC_000016.9Chr1684,629,54784,629,665

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)
nssv17708336<0.00136404
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