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nsv5557204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
Submitted genomic69,322,062-69,322,113Question Mark
Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):67,318,203-67,318,254Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5557204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1769,322,06269,322,113
nsv5557204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1767,318,20367,318,254

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714271line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714271Submitted genomicNC_000017.11:g.693
22062_69322113ins6
019
GRCh38 (hg38)NC_000017.11Chr1769,322,06269,322,113
nssv17714271RemappedPerfectNC_000017.10:g.673
18203_67318254ins6
019
GRCh37.p13First PassNC_000017.10Chr1767,318,20367,318,254

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)
nssv17714271<0.00116404
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