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nsv5563827

  • 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: 114 SVs from 26 studies. See in: genome view    
Submitted genomic39,293,520-39,293,571Question Mark
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):39,762,724-39,762,775Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1439,293,52039,293,571
nsv5563827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1439,762,72439,762,775

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696531line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696531Submitted genomicNC_000014.9:g.3929
3520_39293571ins60
16
GRCh38 (hg38)NC_000014.9Chr1439,293,52039,293,571
nssv17696531RemappedPerfectNC_000014.8:g.3976
2724_39762775ins60
16
GRCh37.p13First PassNC_000014.8Chr1439,762,72439,762,775

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)
nssv17696531<0.00116404
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