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nsv5546853

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,741

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 16 studies. See in: genome view    
Submitted genomic34,181,129-34,183,869Question Mark
Overlapping variant regions from other studies: 138 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):35,553,430-35,556,170Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546853Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2134,181,12934,183,869
nsv5546853RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2135,553,43035,556,170

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734710duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734710Submitted genomicNC_000021.9:g.3418
1129_34183869dup
GRCh38 (hg38)NC_000021.9Chr2134,181,12934,183,869
nssv17734710RemappedPerfectNC_000021.8:g.3555
3430_35556170dup
GRCh37.p13First PassNC_000021.8Chr2135,553,43035,556,170

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)
nssv17734710<0.00126404
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