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nsv5533038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,677

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 523 SVs from 52 studies. See in: genome view    
Submitted genomic63,087,669-63,253,345Question Mark
Overlapping variant regions from other studies: 523 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):63,379,868-63,545,544Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1563,087,66963,253,345
nsv5533038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1563,379,86863,545,544

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702853duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702853Submitted genomicNC_000015.10:g.630
87669_63253345dup
GRCh38 (hg38)NC_000015.10Chr1563,087,66963,253,345
nssv17702853RemappedPerfectNC_000015.9:g.6337
9868_63545544dup
GRCh37.p13First PassNC_000015.9Chr1563,379,86863,545,544

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)
nssv17702853<0.00136404
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