U.S. flag

An official website of the United States government

nsv5422062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
Submitted genomic51,076,835-51,076,886Question Mark
Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):51,470,618-51,470,669Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,076,83551,076,886
nsv5422062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,470,61851,470,669

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058555alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058555Submitted genomicNC_000012.12:g.510
76835_51076886ins2
53
GRCh38 (hg38)NC_000012.12Chr1251,076,83551,076,886
nssv17058555RemappedPerfectNC_000012.11:g.514
70618_51470669ins2
53
GRCh37.p13First PassNC_000012.11Chr1251,470,61851,470,669

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)
nssv17058555<0.00126404
Support Center