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nsv5495067

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:778

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
Submitted genomic53,316,498-53,317,275Question Mark
Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):53,710,282-53,711,059Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495067Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,316,49853,317,275
nsv5495067RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,710,28253,711,059

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058661deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058661Submitted genomicNC_000012.12:g.533
16498_53317275del
GRCh38 (hg38)NC_000012.12Chr1253,316,49853,317,275
nssv17058661RemappedPerfectNC_000012.11:g.537
10282_53711059del
GRCh37.p13First PassNC_000012.11Chr1253,710,28253,711,059

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)
nssv17058661<0.00126404
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