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nsv5554909

  • 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: 175 SVs from 32 studies. See in: genome view    
Submitted genomic17,700,554-17,700,605Question Mark
Overlapping variant regions from other studies: 175 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):17,700,785-17,700,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554909Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr617,700,55417,700,605
nsv5554909RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr617,700,78517,700,836

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979227sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979227Submitted genomicNC_000006.12:g.177
00554_17700605ins7
00
GRCh38 (hg38)NC_000006.12Chr617,700,55417,700,605
nssv16979227RemappedPerfectNC_000006.11:g.177
00785_17700836ins7
00
GRCh37.p13First PassNC_000006.11Chr617,700,78517,700,836

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)
nssv16979227<0.00116404
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