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nsv5904980

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
Submitted genomic170,012,229-170,012,285Question Mark
Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):169,439,233-169,439,289Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5904980Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,012,229170,012,285
nsv5904980RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5169,439,233169,439,289

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17425397deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17425397Submitted genomicNC_000005.10:g.170
012229_170012285de
l
GRCh38 (hg38)NC_000005.10Chr5170,012,229170,012,285
nssv17425397RemappedPerfectNC_000005.9:g.1694
39233_169439289del
GRCh37.p13First PassNC_000005.9Chr5169,439,233169,439,289

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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