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nsv5502719

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:421

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 26 studies. See in: genome view    
Submitted genomic10,700,817-10,701,237Question Mark
Overlapping variant regions from other studies: 124 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):10,853,416-10,853,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502719Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1210,700,81710,701,237
nsv5502719RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,853,41610,853,836

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053056deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053056Submitted genomicNC_000012.12:g.107
00817_10701237del
GRCh38 (hg38)NC_000012.12Chr1210,700,81710,701,237
nssv17053056RemappedPerfectNC_000012.11:g.108
53416_10853836del
GRCh37.p13First PassNC_000012.11Chr1210,853,41610,853,836

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)
nssv17053056<0.00126404
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