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nsv5498104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,710

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 557 SVs from 61 studies. See in: genome view    
Submitted genomic52,294,714-52,389,423Question Mark
Overlapping variant regions from other studies: 557 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):52,688,498-52,783,207Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,294,71452,389,423
nsv5498104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,688,49852,783,207

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058764duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058764Submitted genomicNC_000012.12:g.522
94714_52389423dup
GRCh38 (hg38)NC_000012.12Chr1252,294,71452,389,423
nssv17058764RemappedPerfectNC_000012.11:g.526
88498_52783207dup
GRCh37.p13First PassNC_000012.11Chr1252,688,49852,783,207

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)
nssv17058764<0.00146404
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