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nsv5517411

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,930

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 240 SVs from 43 studies. See in: genome view    
Submitted genomic63,261,644-63,267,573Question Mark
Overlapping variant regions from other studies: 240 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):61,892,996-61,898,925Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517411Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,261,64463,267,573
nsv5517411RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,892,99661,898,925

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733649deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733649Submitted genomicNC_000020.11:g.632
61644_63267573del
GRCh38 (hg38)NC_000020.11Chr2063,261,64463,267,573
nssv17733649RemappedPerfectNC_000020.10:g.618
92996_61898925del
GRCh37.p13First PassNC_000020.10Chr2061,892,99661,898,925

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)
nssv17733649<0.00126404
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