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nsv5496788

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,723

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 35 studies. See in: genome view    
Submitted genomic50,455,516-50,457,238Question Mark
Overlapping variant regions from other studies: 98 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):50,849,299-50,851,021Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496788Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1250,455,51650,457,238
nsv5496788RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1250,849,29950,851,021

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056494deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056494Submitted genomicNC_000012.12:g.504
55516_50457238del
GRCh38 (hg38)NC_000012.12Chr1250,455,51650,457,238
nssv17056494RemappedPerfectNC_000012.11:g.508
49299_50851021del
GRCh37.p13First PassNC_000012.11Chr1250,849,29950,851,021

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)
nssv17056494<0.00126404
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