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nsv5497696

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,342

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 25 studies. See in: genome view    
Submitted genomic49,256,147-49,257,488Question Mark
Overlapping variant regions from other studies: 170 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):49,830,283-49,831,624Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5497696Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1349,256,14749,257,488
nsv5497696RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1349,830,28349,831,624

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687623deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687623Submitted genomicNC_000013.11:g.492
56147_49257488del
GRCh38 (hg38)NC_000013.11Chr1349,256,14749,257,488
nssv17687623RemappedPerfectNC_000013.10:g.498
30283_49831624del
GRCh37.p13First PassNC_000013.10Chr1349,830,28349,831,624

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)
nssv17687623<0.00116404
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