U.S. flag

An official website of the United States government

nsv5513210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,871

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 386 SVs from 48 studies. See in: genome view    
Submitted genomic124,332,483-124,404,353Question Mark
Overlapping variant regions from other studies: 386 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):124,202,379-124,274,249Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5513210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,332,483124,404,353
nsv5513210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,202,379124,274,249

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053684deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053684Submitted genomicNC_000011.10:g.124
332483_124404353de
l
GRCh38 (hg38)NC_000011.10Chr11124,332,483124,404,353
nssv17053684RemappedPerfectNC_000011.9:g.1242
02379_124274249del
GRCh37.p13First PassNC_000011.9Chr11124,202,379124,274,249

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)
nssv17053684<0.00126404
Support Center