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nsv5496630

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 25 studies. See in: genome view    
Submitted genomic49,917,451-49,917,535Question Mark
Overlapping variant regions from other studies: 183 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):50,491,587-50,491,671Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1349,917,45149,917,535
nsv5496630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1350,491,58750,491,671

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687671deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687671Submitted genomicNC_000013.11:g.499
17451_49917535del
GRCh38 (hg38)NC_000013.11Chr1349,917,45149,917,535
nssv17687671RemappedPerfectNC_000013.10:g.504
91587_50491671del
GRCh37.p13First PassNC_000013.10Chr1350,491,58750,491,671

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)
nssv176876710.002126404
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