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nsv5485338

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:704

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 19 studies. See in: genome view    
Submitted genomic66,427,917-66,428,620Question Mark
Overlapping variant regions from other studies: 117 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):67,340,152-67,340,855Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485338Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr866,427,91766,428,620
nsv5485338RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr867,340,15267,340,855

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17013735deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17013735Submitted genomicNC_000008.11:g.664
27917_66428620del
GRCh38 (hg38)NC_000008.11Chr866,427,91766,428,620
nssv17013735RemappedPerfectNC_000008.10:g.673
40152_67340855del
GRCh37.p13First PassNC_000008.10Chr867,340,15267,340,855

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)
nssv17013735<0.00126404
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