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nsv5481612

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,183

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 210 SVs from 22 studies. See in: genome view    
Submitted genomic18,088,861-18,090,043Question Mark
Overlapping variant regions from other studies: 210 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):17,946,370-17,947,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481612Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr818,088,86118,090,043
nsv5481612RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,946,37017,947,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008948deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008948Submitted genomicNC_000008.11:g.180
88861_18090043del
GRCh38 (hg38)NC_000008.11Chr818,088,86118,090,043
nssv17008948RemappedPerfectNC_000008.10:g.179
46370_17947552del
GRCh37.p13First PassNC_000008.10Chr817,946,37017,947,552

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)
nssv17008948<0.00126404
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