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nsv5533342

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:696

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 29 studies. See in: genome view    
Submitted genomic67,218,892-67,219,587Question Mark
Overlapping variant regions from other studies: 124 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):67,252,795-67,253,490Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533342Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,218,89267,219,587
nsv5533342RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,252,79567,253,490

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707486deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707486Submitted genomicNC_000016.10:g.672
18892_67219587del
GRCh38 (hg38)NC_000016.10Chr1667,218,89267,219,587
nssv17707486RemappedPerfectNC_000016.9:g.6725
2795_67253490del
GRCh37.p13First PassNC_000016.9Chr1667,252,79567,253,490

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)
nssv17707486<0.00126404
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