U.S. flag

An official website of the United States government

nsv5481670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,213

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 23 studies. See in: genome view    
Submitted genomic43,391,155-43,392,367Question Mark
Overlapping variant regions from other studies: 75 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):43,886,603-43,887,815Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1043,391,15543,392,367
nsv5481670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1043,886,60343,887,815

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17032757deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17032757Submitted genomicNC_000010.11:g.433
91155_43392367del
GRCh38 (hg38)NC_000010.11Chr1043,391,15543,392,367
nssv17032757RemappedPerfectNC_000010.10:g.438
86603_43887815del
GRCh37.p13First PassNC_000010.10Chr1043,886,60343,887,815

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)
nssv17032757<0.00156404
Support Center