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nsv5473207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
Submitted genomic39,300,480-39,300,605Question Mark
Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):39,300,582-39,300,707Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473207Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,300,48039,300,605
nsv5473207RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,300,58239,300,707

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964285duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964285Submitted genomicNC_000005.10:g.393
00480_39300605dup
GRCh38 (hg38)NC_000005.10Chr539,300,48039,300,605
nssv16964285RemappedPerfectNC_000005.9:g.3930
0582_39300707dup
GRCh37.p13First PassNC_000005.9Chr539,300,58239,300,707

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)
nssv16964285<0.00136404
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