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nsv5523859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:673

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 456 SVs from 42 studies. See in: genome view    
Submitted genomic80,070,806-80,071,478Question Mark
Overlapping variant regions from other studies: 453 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):77,830,806-77,831,478Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1880,070,80680,071,478
nsv5523859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1877,830,80677,831,478

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17719988deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17719988Submitted genomicNC_000018.10:g.800
70806_80071478del
GRCh38 (hg38)NC_000018.10Chr1880,070,80680,071,478
nssv17719988RemappedPerfectNC_000018.9:g.7783
0806_77831478del
GRCh37.p13First PassNC_000018.9Chr1877,830,80677,831,478

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)
nssv177199880.1026416300
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