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nsv5504086

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 28 studies. See in: genome view    
Submitted genomic47,683,695-47,684,026Question Mark
Overlapping variant regions from other studies: 94 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):47,705,247-47,705,578Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504086Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1147,683,69547,684,026
nsv5504086RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1147,705,24747,705,578

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17045375deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17045375Submitted genomicNC_000011.10:g.476
83695_47684026del
GRCh38 (hg38)NC_000011.10Chr1147,683,69547,684,026
nssv17045375RemappedPerfectNC_000011.9:g.4770
5247_47705578del
GRCh37.p13First PassNC_000011.9Chr1147,705,24747,705,578

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)
nssv17045375<0.00116404
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