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nsv5528091

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,079

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 33 studies. See in: genome view    
Submitted genomic81,849,376-81,853,454Question Mark
Overlapping variant regions from other studies: 188 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):79,807,252-79,811,330Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528091Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1781,849,37681,853,454
nsv5528091RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1779,807,25279,811,330

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715616deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715616Submitted genomicNC_000017.11:g.818
49376_81853454del
GRCh38 (hg38)NC_000017.11Chr1781,849,37681,853,454
nssv17715616RemappedPerfectNC_000017.10:g.798
07252_79811330del
GRCh37.p13First PassNC_000017.10Chr1779,807,25279,811,330

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)
nssv17715616<0.00126404
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