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nsv5489549

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,485

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 33 studies. See in: genome view    
Submitted genomic99,661,966-99,688,450Question Mark
Overlapping variant regions from other studies: 154 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):101,421,723-101,448,207Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489549Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1099,661,96699,688,450
nsv5489549RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10101,421,723101,448,207

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17039842deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17039842Submitted genomicNC_000010.11:g.996
61966_99688450del
GRCh38 (hg38)NC_000010.11Chr1099,661,96699,688,450
nssv17039842RemappedPerfectNC_000010.10:g.101
421723_101448207de
l
GRCh37.p13First PassNC_000010.10Chr10101,421,723101,448,207

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)
nssv17039842<0.00116404
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