U.S. flag

An official website of the United States government

nsv5457382

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 68 SVs from 15 studies. See in: genome view    
Submitted genomic173,139,560-173,139,631Question Mark
Overlapping variant regions from other studies: 68 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):172,566,563-172,566,634Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457382Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5173,139,560173,139,631
nsv5457382RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5172,566,563172,566,634

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978659duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978659Submitted genomicNC_000005.10:g.173
139560_173139631du
p
GRCh38 (hg38)NC_000005.10Chr5173,139,560173,139,631
nssv16978659RemappedPerfectNC_000005.9:g.1725
66563_172566634dup
GRCh37.p13First PassNC_000005.9Chr5172,566,563172,566,634

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)
nssv16978659<0.00116404
Support Center