U.S. flag

An official website of the United States government

nsv5508471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,643

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 23 studies. See in: genome view    
Submitted genomic41,108,039-41,111,681Question Mark
Overlapping variant regions from other studies: 97 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):41,400,237-41,403,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,108,03941,111,681
nsv5508471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,400,23741,403,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700161deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700161Submitted genomicNC_000015.10:g.411
08039_41111681del
GRCh38 (hg38)NC_000015.10Chr1541,108,03941,111,681
nssv17700161RemappedPerfectNC_000015.9:g.4140
0237_41403879del
GRCh37.p13First PassNC_000015.9Chr1541,400,23741,403,879

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)
nssv17700161<0.00126404
Support Center