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nsv5477452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
Submitted genomic47,796,726-47,796,844Question Mark
Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):48,709,287-48,709,405Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477452Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr847,796,72647,796,844
nsv5477452RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr848,709,28748,709,405

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17010817deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17010817Submitted genomicNC_000008.11:g.477
96726_47796844del
GRCh38 (hg38)NC_000008.11Chr847,796,72647,796,844
nssv17010817RemappedPerfectNC_000008.10:g.487
09287_48709405del
GRCh37.p13First PassNC_000008.10Chr848,709,28748,709,405

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)
nssv17010817<0.00136404
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