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nsv5470436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,167

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 232 SVs from 44 studies. See in: genome view    
Submitted genomic94,127,706-94,176,872Question Mark
Overlapping variant regions from other studies: 232 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):95,048,857-95,098,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr494,127,70694,176,872
nsv5470436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr495,048,85795,098,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952774deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952774Submitted genomicNC_000004.12:g.941
27706_94176872del
GRCh38 (hg38)NC_000004.12Chr494,127,70694,176,872
nssv16952774RemappedPerfectNC_000004.11:g.950
48857_95098023del
GRCh37.p13First PassNC_000004.11Chr495,048,85795,098,023

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)
nssv16952774<0.00116404
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