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nsv5511910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,369

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 40 studies. See in: genome view    
Submitted genomic47,740,318-47,741,686Question Mark
Overlapping variant regions from other studies: 119 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):47,761,870-47,763,238Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5511910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1147,740,31847,741,686
nsv5511910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1147,761,87047,763,238

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17045379deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17045379Submitted genomicNC_000011.10:g.477
40318_47741686del
GRCh38 (hg38)NC_000011.10Chr1147,740,31847,741,686
nssv17045379RemappedPerfectNC_000011.9:g.4776
1870_47763238del
GRCh37.p13First PassNC_000011.9Chr1147,761,87047,763,238

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)
nssv170453790.0161036404
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