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nsv5473430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,325

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 600 SVs from 75 studies. See in: genome view    
Submitted genomic181,061,000-181,100,324Question Mark
Overlapping variant regions from other studies: 600 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):180,488,000-180,527,324Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,061,000181,100,324
nsv5473430RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,488,000180,527,324

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978352duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978352Submitted genomicNC_000005.10:g.181
061000_181100324du
p
GRCh38 (hg38)NC_000005.10Chr5181,061,000181,100,324
nssv16978352RemappedPerfectNC_000005.9:g.1804
88000_180527324dup
GRCh37.p13First PassNC_000005.9Chr5180,488,000180,527,324

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)
nssv16978352<0.00126404
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