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nsv5499592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:496,631

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2951 SVs from 95 studies. See in: genome view    
Submitted genomic1,387,775-1,884,405Question Mark
Overlapping variant regions from other studies: 2951 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):1,409,005-1,905,635Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr111,387,7751,884,405
nsv5499592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,409,0051,905,635

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17042058duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17042058Submitted genomicNC_000011.10:g.138
7775_1884405dup
GRCh38 (hg38)NC_000011.10Chr111,387,7751,884,405
nssv17042058RemappedPerfectNC_000011.9:g.1409
005_1905635dup
GRCh37.p13First PassNC_000011.9Chr111,409,0051,905,635

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)
nssv17042058<0.00146404
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