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nsv5470893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:475

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
Submitted genomic36,898,120-36,898,594Question Mark
Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):36,865,896-36,866,370Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr636,898,12036,898,594
nsv5470893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr636,865,89636,866,370

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982091deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982091Submitted genomicNC_000006.12:g.368
98120_36898594del
GRCh38 (hg38)NC_000006.12Chr636,898,12036,898,594
nssv16982091RemappedPerfectNC_000006.11:g.368
65896_36866370del
GRCh37.p13First PassNC_000006.11Chr636,865,89636,866,370

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)
nssv16982091<0.00126404
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