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nsv5462109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:601,461

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2009 SVs from 75 studies. See in: genome view    
Submitted genomic175,785,135-176,386,595Question Mark
Overlapping variant regions from other studies: 2009 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):176,706,286-177,307,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5462109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4175,785,135176,386,595
nsv5462109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4176,706,286177,307,746

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16960214duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16960214Submitted genomicNC_000004.12:g.175
785135_176386595du
p
GRCh38 (hg38)NC_000004.12Chr4175,785,135176,386,595
nssv16960214RemappedPerfectNC_000004.11:g.176
706286_177307746du
p
GRCh37.p13First PassNC_000004.11Chr4176,706,286177,307,746

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)
nssv16960214<0.00126404
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