U.S. flag

An official website of the United States government

nsv5538388

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 67 SVs from 16 studies. See in: genome view    
Submitted genomic39,968,164-39,968,234Question Mark
Overlapping variant regions from other studies: 67 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):40,364,168-40,364,238Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538388Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2239,968,16439,968,234
nsv5538388RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2240,364,16840,364,238

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729041duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729041Submitted genomicNC_000022.11:g.399
68164_39968234dup
GRCh38 (hg38)NC_000022.11Chr2239,968,16439,968,234
nssv17729041RemappedPerfectNC_000022.10:g.403
64168_40364238dup
GRCh37.p13First PassNC_000022.10Chr2240,364,16840,364,238

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)
nssv17729041<0.00126404
Support Center