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nsv5469776

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,570

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 203 SVs from 36 studies. See in: genome view    
Submitted genomic126,767,091-126,787,660Question Mark
Overlapping variant regions from other studies: 203 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):126,102,783-126,123,352Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5469776Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5126,767,091126,787,660
nsv5469776RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5126,102,783126,123,352

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973490deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973490Submitted genomicNC_000005.10:g.126
767091_126787660de
l
GRCh38 (hg38)NC_000005.10Chr5126,767,091126,787,660
nssv16973490RemappedPerfectNC_000005.9:g.1261
02783_126123352del
GRCh37.p13First PassNC_000005.9Chr5126,102,783126,123,352

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)
nssv16973490<0.00116404
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